FDA Inspection 1053027 — Cryopen, LLC
The FDA completed an inspection of Cryopen, LLC on Mar 13, 2018 in Covington, LA. 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
- Mar 13, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Covington, LA (United States)