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Code · STATUTE-COMPILATIONS · FDA Reauthorization Act of 2017 · Sec. 204

Sec. 204. REAUTHORIZATION; REPORTING REQUIREMENTS

150 words·~1 min read·/statute-compilations/comps-15234/sec-204

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## SEC. 204 REAUTHORIZATION; REPORTING REQUIREMENTS ###
(a)Performance Reports Section 738A(a) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379j-1(a)) is amended— ####
(1)in paragraph (1)— #####
(A)in subparagraph (A)— ######
(i)by striking “2013” and inserting “2018”; and ######
(ii)by striking “the Medical Device User Fee Amendments of 2012” and inserting “the Medical Device User Fee Amendments of 2017”; and #####
(B)in subparagraph (B), by striking “the Medical Device User Fee Amendments Act of 2012” and inserting “the Medical Device User Fee Amendments of 2017”; and ####
(2)in paragraph (2), by striking “2013 through 2017” and inserting “2018 through 2022”. ###
(b)Reauthorization Section 738A(b) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379j-1(b)) is amended— ####
(1)in paragraph (1), by striking “2017” and inserting “2022”; and ####
(2)in paragraph (5), by striking “2017” and inserting “2022”.
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Sec. 204
REAUTHORIZATION; REPORTING REQUIREMENTS
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