FDA Inspection 557909 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on January 15, 2009 in Wichita Falls, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- January 15, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Wichita Falls, TX (United States)