FDA Inspection 1022503 — Integra Lifescience, LLC

Integra Lifescience, LLC — FEI 1938191

The FDA completed an inspection of Integra Lifescience, LLC on August 14, 2017 in Fenton, MO. 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
August 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fenton, MO (United States)