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Guidance for Industry and FDA Staff - Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002,
ICR 202106-0910-007 · OMB 0910-0485 · Object 112460201.
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Document Metadata
| File Type | application/pdf |
|---|---|
| File Title | Guidance for Industry and FDA Staff - Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, |
| Subject | Issued: 05-01-2006 |
| Author | Casper Uldriks |
| File Modified | 2015-06-29 |
| File Created | 2006-04-28 |
| Conversion State | complete |