FDA Inspection
UMTBUMTB – FDA Inspection, Nov 20, 2012
Record Details
This FDA Inspection record concerns UMTB, with an inspection on November 20, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- UMTB
- Inspection Date
- November 20, 2012
- Product Type
- Biologics
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ID · 8f691150-3833-4ff1-b04a-50599275d046
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 810356
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.200(e)Documentation of maintenance and cleaning
- 21 CFR 1271.190(d)(2)Documentation of activities
- 21 CFR 1271.190(d)(1)Procedures for cleaning, sanitation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of UMTB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 15, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for UMTB
- FDA Inspection 907108 - 2014-12-15
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