FDA Inspection
Apixia IncApixia Inc – FDA Inspection, Feb 14, 2019
Record Details
This FDA Inspection record concerns Apixia Inc, with an inspection on February 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d348da92-f65c-44a1-a67c-bddb03b79b27
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1079324
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
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Other FDA inspections of Apixia Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 11, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 7, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Apixia Inc
- FDA Inspection 932609 - 2015-06-11
- FDA Inspection 747017 - 2011-09-07
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