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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 201504-0910-002 · OMB 0910-0577 · Object 54755001.
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Document Metadata
| File Type | application/octet-stream |
|---|---|
| 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 | 2012-02-06 |
| File Created | 2006-04-28 |
| Conversion State | complete |