FDA Inspection 673198 — Organogenesis, Inc.

Organogenesis, Inc. — FEI 1000148471

The FDA completed an inspection of Organogenesis, Inc. on Jul 27, 2010 in Canton, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Canton, MA (United States)

Citations

IDCFRDescription
341521 CFR 820.22Quality Audit/Reaudit - conducted