FDA Inspection
AlloSourceAlloSource – FDA Inspection, May 7, 2010
Record Details
This FDA Inspection record concerns AlloSource, with an inspection on May 7, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- AlloSource
- Inspection Date
- May 7, 2010
- Product Type
- Devices
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ID · f2b1a590-4f24-4eb8-8ceb-cd7321b87e65
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 664318
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 1271.370(b)(1)Identification code affixed
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Other FDA inspections of AlloSource
8| Date | Classification | Office | Project area |
|---|---|---|---|
| August 28, 2026 | Not classified | Denver District Office | Human Cellular, Tissue, and Gene Therapies |
| March 30, 2023 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| July 27, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 18, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 9, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for AlloSource
- FDA Inspection 1333098 - 2026-08-28
- FDA Inspection 1201259 - 2023-03-30
- FDA Inspection 1175639 - 2022-07-27
- FDA Inspection 1074854 - 2018-12-18
- FDA Inspection 1010063 - 2017-02-09
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