FDA Inspection
Apixia IncApixia Inc – FDA Inspection, Sep 7, 2011
Record Details
This FDA Inspection record concerns Apixia Inc, with an inspection on September 7, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Apixia Inc
- Inspection Date
- September 7, 2011
- Product Type
- Devices
View Company Profile
ID · 15e2981a-53ed-4306-bf92-9df6188c61b4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 747017
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Apixia Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 14, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 11, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Apixia Inc
- FDA Inspection 1079324 - 2019-02-14
- FDA Inspection 932609 - 2015-06-11
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