FDA Inspection
NAMSANAMSA – FDA Inspection, May 18, 2018
Record Details
This FDA Inspection record concerns NAMSA, with an inspection on May 18, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · abf563d6-f014-4fbf-9ec9-0964b6e04e07
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1052433
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 812.40Sponsors" general responsibilities
- 21 CFR 812.40Sponsors' general responsibilities
Full citation text and observation details available on the Dashboard.
Other FDA inspections of NAMSA
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 16, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 4, 2013 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 3, 2010 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for NAMSA
- FDA Inspection 1197992 - 2023-02-08
- FDA Inspection 1002871 - 2017-02-16
- FDA Inspection 819156 - 2013-02-04
- FDA Inspection 676437 - 2010-09-03
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