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Document 22013D0184

    Decision of the EEA Joint Committee No 184/2013 of 8 November 2013 amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

    OJ L 92, 27.3.2014, p. 9–9 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    Legal status of the document In force

    ELI: http://data.europa.eu/eli/dec/2013/184(2)/oj

    Date of document:
    08/11/2013
    Date of effect:
    09/11/2013; Entry into force See Art 4
    Date of end of validity:
    No end date
    Author:
    EEA Joint Committee
    Form:
    Decision adopted by bodies created by international agreements
    Treaty:
    Agreement on the European Economic Area
    Legal basis:
    Link
    Link
    Link
    Select all documents mentioning this document
    Modifies:
    Relation Act Comment Subdivision concerned From To
    Modifies 21994A0103(51) Addition chapter II point 40 indent 09/11/2013
    Modifies 21994A0103(52) Addition chapter XII point 54zzy indent 09/11/2013
    Instruments cited:
    Link

    27.3.2014   

    EN

    Official Journal of the European Union

    L 92/9

    DECISION OF THE EEA JOINT COMMITTEE

    No 184/2013

    of 8 November 2013

    amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

    THE EEA JOINT COMMITTEE,

    Having regard to the Agreement on the European Economic Area (‘the EEA Agreement’), and in particular Article 98 thereof,

    Whereas:

    (1)

    Commission Regulation (EU) No 34/2013 of 16 January 2013 amending Annexes II, III and IV to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for 2-phenylphenol, ametoctradin, Aureobasidium pullulans strains DSM 14940 and DSM 14941, cyproconazole, difenoconazole, dithiocarbamates, folpet, propamocarb, spinosad, spirodiclofen, tebufenpyrad and tetraconazole in or on certain products (1) is to be incorporated into the EEA Agreement.

    (2)

    Commission Regulation (EU) No 35/2013 of 18 January 2013 amending Annexes II and III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for dimethomorph, indoxacarb, pyraclostrobin and trifloxystrobin in or on certain products (2) is to be incorporated into the EEA Agreement.

    (3)

    This Decision concerns legislation regarding feedingstuffs and foodstuffs. Legislation regarding feedingstuffs and foodstuffs shall not apply to Liechtenstein as long as the application of the Agreement between the European Community and the Swiss Confederation on trade in agricultural products is extended to Liechtenstein, as specified in the sectoral adaptations to Annex I and the introduction to Chapter XII of Annex II to the EEA Agreement. This Decision is therefore not to apply to Liechtenstein.

    (4)

    Annexes I and II to the EEA Agreement should therefore be amended accordingly,

    HAS ADOPTED THIS DECISION:

    Article 1

    The following indents are added in point 40 (Regulation (EC) No 396/2005 of the European Parliament and of the Council) of Chapter II of Annex I to the EEA Agreement:

    ‘—

    32013 R 0034: Commission Regulation (EU) No 34/2013 of 16 January 2013 (OJ L 25, 26.1.2013, p. 1),

    —

    32013 R 0035: Commission Regulation (EU) No 35/2013 of 18 January 2013 (OJ L 25, 26.1.2013, p. 49).’.

    Article 2

    The following indents are added in point 54zzy (Regulation (EC) No 396/2005 of the European Parliament and of the Council) of Chapter XII of Annex II to the EEA Agreement:

    ‘—

    32013 R 0034: Commission Regulation (EU) No 34/2013 of 16 January 2013 (OJ L 25, 26.1.2013, p. 1),

    —

    32013 R 0035: Commission Regulation (EU) No 35/2013 of 18 January 2013 (OJ L 25, 26.1.2013, p. 49).’.

    Article 3

    The texts of Regulations (EU) No 34/2013 and (EU) No 35/2013 in the Icelandic and Norwegian languages, to be published in the EEA Supplement to the Official Journal of the European Union, shall be authentic.

    Article 4

    This Decision shall enter into force on 9 November 2013, provided that all the notifications under Article 103(1) of the EEA Agreement have been made (*1).

    Article 5

    This Decision shall be published in the EEA Section of, and in the EEA Supplement to, the Official Journal of the European Union.

    Done at Brussels, 8 November 2013.

    For the EEA Joint Committee

    The President

    Thórir IBSEN

    (1)   OJ L 25, 26.1.2013, p. 1.

    (2)   OJ L 25, 26.1.2013, p. 49.

    (*1)  No constitutional requirements indicated.

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