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Guide for Preparing Product Reports on Sunlamps and Sunlamp Products
분류 Molecular imaging, Guidance 조회 2704
발행년도 2014 등록일 2015-10-02
출처 FDA (바로가기)
Sunlamp Product Reports, Supplemental Reports, and Abbreviated Reports must be submitted to the Center for Devices and Radiological Health (CDRH) at the address below prior to introduction of the products into U.S. commerce.
 
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리스트 이전글과 다음글
이전글이전글 Guide for Preparing Annual Reports on Radiation Safety Testing of Mercury Vapor Lamps
다음글다음글 Guide for Preparing Annual Reports on Radiation Safety Testing of Sunlamps and Sunlamp Products