FDA Inspection
Augmenix IncAugmenix Inc – FDA Inspection, Oct 17, 2014
Record Details
This FDA Inspection record concerns Augmenix Inc, with an inspection on October 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Augmenix Inc
- Inspection Date
- October 17, 2014
- Product Type
- Devices
View Company Profile
ID · 26ec868d-6d6d-4668-8576-3cff6eb1d8aa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 901350
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.75(a)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Augmenix Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2019 | Not classified | New England District Office | |
| January 12, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Augmenix Inc
- FDA Inspection 1159303 - 2019-05-22
- FDA Inspection 762778 - 2012-01-12
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