FDA Inspection 1000745 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on February 7, 2017 in Orem, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 7, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Orem, UT (United States)