FDA Inspection 800788 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on Sep 20, 2012 in Lancaster, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 20, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lancaster, TX (United States)