FDA Inspection 671599 — Eurofins Viracor, LLC.
The FDA completed an inspection of Eurofins Viracor, LLC. on Jul 8, 2010 in Lenexa, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 8, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Lenexa, KS (United States)
Additional Details
Clinical Investigator (CI)