FDA Inspection 1030569 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on October 24, 2017 in Corpus Christi, TX. 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
- October 24, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Corpus Christi, TX (United States)