FDA Inspection 1097262 — Biolife, LLC

Biolife, LLC — FEI 3003395204

The FDA completed an inspection of Biolife, LLC on May 15, 2019 in Sarasota, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 15, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Sarasota, FL (United States)