FDA Inspection 681385 — Biomat USA Inc.
The FDA completed an inspection of Biomat USA Inc. on July 30, 2010 in Sioux Falls, SD. 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
- July 30, 2010
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Sioux Falls, SD (United States)