FDA Inspection
AlloSourceAlloSource – FDA Inspection, May 26, 2009
Record Details
This FDA Inspection record concerns AlloSource, with an inspection on May 26, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- AlloSource
- Inspection Date
- May 26, 2009
- Product Type
- Biologics
View Company Profile
ID · 1160463e-4450-4e36-808b-959578e90975
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 584607
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
4- 21 CFR 1271.200(a)Design appropriate, suitably located
- 21 CFR 1271.160(b)(6)Deviations--evaluation, cause, corrective action
- 21 CFR 1271.47(a)Procedures for all other requirements
- 21 CFR 1271.270(a)Records maintained concurrently
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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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