FDA Inspection 1021261 — Collagen Matrix, Inc.

Collagen Matrix, Inc. — FEI 3003300673

The FDA completed an inspection of Collagen Matrix, Inc. on July 13, 2017 in Allendale, NJ. 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
July 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Allendale, NJ (United States)