FDA Inspection
Unicare Biomedical, Inc.Unicare Biomedical, Inc. – FDA Inspection, May 9, 2013
Record Details
This FDA Inspection record concerns Unicare Biomedical, Inc., with an inspection on May 9, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Unicare Biomedical, Inc.
- Inspection Date
- May 9, 2013
- Product Type
- Devices
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ID · e4739503-59ee-4ec5-a813-2704864fdce2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 830902
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
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Other FDA inspections of Unicare Biomedical, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 28, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 6, 2024 | Not classified | Los Angeles District Office | |
| June 28, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 11, 2022 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| April 13, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Unicare Biomedical, Inc.
- FDA Inspection 1329140 - 2026-07-28
- FDA Inspection 1234094 - 2024-03-06
- FDA Inspection 1174261 - 2022-06-28
- FDA Inspection 1169384 - 2022-05-11
- FDA Inspection 974365 - 2016-04-13
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