FDA Inspection
MVF LLCMVF LLC – FDA Inspection, Jan 19, 2011
Record Details
This FDA Inspection record concerns MVF LLC, with an inspection on January 19, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- MVF LLC
- Inspection Date
- January 19, 2011
- Product Type
- Biologics
View Company Profile
ID · 97141843-88d9-40f8-8df9-83de0640b065
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 706920
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.47(a)Procedures for all other requirements
- 21 CFR 1271.55(b)(1)Statement re: certified testing lab
- 21 CFR 1271.55(b)(3)Name and address on summary
Full citation text and observation details available on the Dashboard.
Other FDA inspections of MVF LLC
9| Date | Classification | Office | Project area |
|---|---|---|---|
| January 31, 2025 | Not classified | Denver District Office | |
| April 12, 2021 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 6, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 22, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 26, 2016 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for MVF LLC
- FDA Inspection 1260121 - 2025-01-31
- FDA Inspection 1140539 - 2021-04-12
- FDA Inspection 1082772 - 2019-03-06
- FDA Inspection 1071568 - 2018-10-22
- FDA Inspection 989326 - 2016-07-26
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