FDA Inspection
Nanovis LLCNanovis LLC – FDA Inspection, Jul 18, 2018
Record Details
This FDA Inspection record concerns Nanovis LLC, with an inspection on July 18, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f1e966c4-b3ae-4b13-bc7a-137e0a6be586
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059225
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
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Other FDA inspections of Nanovis LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 19, 2026 | OAI | Detroit District Office | Postmarket Assurance: Devices |
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