FDA Inspection 780510 — Organogenesis, Inc.

Organogenesis, Inc. — FEI 1000148471

The FDA completed an inspection of Organogenesis, Inc. on May 7, 2012 in Canton, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 7, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Canton, MA (United States)

Citations

IDCFRDescription
1472121 CFR 820.70(g)(2)Periodic equipment inspections