FDA Inspection
NAMSANAMSA – FDA Inspection, Feb 4, 2013
Record Details
This FDA Inspection record concerns NAMSA, with an inspection on February 4, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- NAMSA
- Inspection Date
- February 4, 2013
- Product Type
- Devices
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ID · 6fc21266-c02e-4542-821a-7d8028eca13b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819156
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(b)(4)(vi)Sponsor lack of other FDA-required info
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 |
| May 18, 2018 | VAI | Center for Devices and Radiological Health | Project Evaluation: Devices |
| February 16, 2017 | NAI | 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 1052433 - 2018-05-18
- FDA Inspection 1002871 - 2017-02-16
- FDA Inspection 676437 - 2010-09-03
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