FDA Inspection
NAMSANAMSA – FDA Inspection, Sep 3, 2010
Record Details
This FDA Inspection record concerns NAMSA, with an inspection on September 3, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- NAMSA
- Inspection Date
- September 3, 2010
- Product Type
- Devices
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ID · edbe69df-7b84-44ef-b60e-8a2feb519632
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 676437
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.43(c)(5)No financial disclosure info in investigator agreement
- 21 CFR 812.43(b)Sponsor shipped devices to unqualified person(s)
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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 |
| February 4, 2013 | 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 819156 - 2013-02-04
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