FDA Inspection
Avioq, Inc.Avioq, Inc. – FDA Inspection, Aug 17, 2017
Record Details
This FDA Inspection record concerns Avioq, Inc., with an inspection on August 17, 2017, issued by the Atlanta District Office, covering medical devices & rad health.
- Company
- Avioq, Inc.
- Inspection Date
- August 17, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Atlanta District Office
View Company Profile
ID · 5512c30c-abc6-4290-88be-18e3140ea5f2
Inspection Facts
- Inspection number
- 1042251
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Avioq, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| May 14, 2026 | Not classified | Atlanta District Office | Blood and Blood Products |
| December 5, 2023 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 27, 2019 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 13, 2017 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 27, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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