FDA Inspection 1067224 — Eurofins Viracor, LLC.
The FDA completed an inspection of Eurofins Viracor, LLC. on September 19, 2018 in Lenexa, KS. 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
- September 19, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Lenexa, KS (United States)