FDA Inspection
Azurity Pharmaceuticals, Inc.Azurity Pharmaceuticals, Inc. – FDA Inspection, Mar 19, 2010
Record Details
This FDA Inspection record concerns Azurity Pharmaceuticals, Inc., with an inspection on March 19, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 19, 2010
- Product Type
- Devices
View Company Profile
ID · 8d81d098-bad2-4c15-a875-ba8c06f04e77
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 655593
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Azurity Pharmaceuticals, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| December 12, 2025 | NAI | Drug Quality Assurance | |
| February 19, 2025 | Not classified | New England District Office | Drug Quality Assurance |
| March 2, 2023 | Not classified | New England District Office | Drug Quality Assurance |
| February 24, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 26, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Azurity Pharmaceuticals, Inc.
- FDA Inspection 1297348 - 2025-12-12
- FDA Inspection 1261303 - 2025-02-19
- FDA Inspection 1199279 - 2023-03-02
- FDA Inspection 1163010 - 2022-02-24
- FDA Inspection 1100022 - 2019-07-26
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.