FDA Inspection 856079 — ACell, Inc

ACell, Inc — FEI 3005920706

The FDA completed an inspection of ACell, Inc on November 20, 2013 in Columbia, MD. 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
November 20, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Columbia, MD (United States)