FDA Inspection 1092596 — Fibrocell Technologies, Inc.

Fibrocell Technologies, Inc. — FEI 3005836954

The FDA completed an inspection of Fibrocell Technologies, Inc. on May 21, 2019 in Exton, PA. 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
May 21, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Exton, PA (United States)

Additional Details

Sponsor, Contract Research Organization