FDA Inspection
Moximed, Inc.Moximed, Inc. – FDA Inspection, Jul 7, 2017
Record Details
This FDA Inspection record concerns Moximed, Inc., with an inspection on July 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Sandra S. Saniga (Issuing Officer)
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ID · b1e6d9c4-ab12-43d8-9a88-da5519f9ecd7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019036
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 812.43(c)No investigator agreement
- 21 CFR 812.40Sponsors" general responsibilities
- 21 CFR 812.43(a)Investigator(s) not qualified
- 21 CFR 812.40Sponsors' general responsibilities
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Other FDA inspections of Moximed, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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