FDA Inspection 776938 — Organogenesis, Inc.

Organogenesis, Inc. — FEI 1000148471

The FDA completed an inspection of Organogenesis, Inc. on Apr 12, 2012 in Canton, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 12, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Canton, MA (United States)