FDA Inspection 808880 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on Nov 30, 2012 in Midwest City, OK. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 30, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Midwest City, OK (United States)