Document
Guidance for Industry, FDA Staff, and Third Parties - Inspection by Accredited Persons Under The Medical Device User Fee and Mod
ICR 201301-0910-011 · OMB 0910-0510 · Object 37574901.
This document may belong to an older filing. More recent activity for OMB 0910-0510:
Document Viewer [pdf]
Status: Original and derived artifacts are available for this document.
Download: pdf
Loading document viewer…
Document Metadata
| File Type | application/octet-stream |
|---|---|
| File Title | Guidance for Industry, FDA Staff, and Third Parties - Inspection by Accredited Persons Under The Medical Device User Fee and Mod |
| Subject | 4 |
| Author | CDRH |
| File Modified | 2012-06-04 |
| File Created | 2009-08-25 |
| Conversion State | complete |