FDA Inspection 545094 — Organogenesis, Inc.

Organogenesis, Inc. — FEI 1000148471

The FDA completed an inspection of Organogenesis, Inc. on Oct 29, 2008 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
Oct 29, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Canton, MA (United States)

Citations

IDCFRDescription
368321 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements