FDA Inspection 643284 — ACell, Inc

ACell, Inc — FEI 3005920706

The FDA completed an inspection of ACell, Inc on February 3, 2010 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
February 3, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MD (United States)