FDA Inspection 993334 — Cryogam Colorado, LLC

Cryogam Colorado, LLC — FEI 3010131527

The FDA completed an inspection of Cryogam Colorado, LLC on Nov 8, 2016 in Denver, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 8, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Denver, CO (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.