# FDA Inspection 810356 - UMTB - November 20, 2012

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

> FDA Inspection 810356 for UMTB on November 20, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

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

## Related Documents

- [FDA Inspection 907108 - 2014-12-15](https://www.keypedia.com/records/fda_inspections/umtb/74ed09ed-1885-422b-a3c1-d2ee245dc584)

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