FDA Inspection
OsteoCentric Technologies, Inc.OsteoCentric Technologies, Inc. – FDA Inspection, Nov 13, 2023
Record Details
This FDA Inspection record concerns OsteoCentric Technologies, Inc., with an inspection on November 13, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d2f65072-0d15-4e1f-88ab-b7eea87cc456
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1222880
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
6- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(a)Complaints
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Other FDA inspections of OsteoCentric Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 30, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for OsteoCentric Technologies, Inc.
- FDA Inspection 983441 - 2016-08-30
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