FDA Inspection
CCRM DFWCCRM DFW – FDA Inspection, Jul 10, 2014
Record Details
This FDA Inspection record concerns CCRM DFW, with an inspection on July 10, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- CCRM DFW
- Inspection Date
- July 10, 2014
- Product Type
- Biologics
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ID · e38cb4f3-6bcc-4e4b-9446-12dad07726fc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 886733
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.60(b)Identified as quarantined, distinguishable
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Other FDA inspections of CCRM DFW
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 4, 2025 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| December 4, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 25, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 25, 2017 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 10, 2014 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for CCRM DFW
- FDA Inspection 1282798 - 2025-09-04
- FDA Inspection 1114052 - 2019-12-04
- FDA Inspection 1023819 - 2017-07-25
- FDA Inspection 1019066 - 2017-07-25
- FDA Inspection 886734 - 2014-07-10
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