FDA Inspection
Nuvasive IncNuvasive Inc – FDA Inspection, Oct 26, 2016
Record Details
This FDA Inspection record concerns Nuvasive Inc, with an inspection on October 26, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c1758c68-3aea-40a5-bf07-cfed24ede39a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 991304
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of Nuvasive Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 27, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nuvasive Inc
- FDA Inspection 892478 - 2014-08-27
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