# UMTB – FDA Inspection, Nov 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/umtb/8f691150-3833-4ff1-b04a-50599275d046
Source feed: FDA_Inspections

> FDA inspection 810356 of UMTB, November 20, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 1271. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 810356
- Company Name: UMTB
- Inspection Date: 2012-11-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 3

## Related Documents

- FDA Inspection 907108 - 2014-12-15

Company: https://www.keypedia.com/companies/umtb/2ff5b284-fcba-47bb-918d-dcd1b31c3276

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d