FDA Inspection 1024981 — Cormed Inc

Cormed Inc — FEI 3012235045

The FDA completed an inspection of Cormed Inc on July 19, 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 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Allendale, NJ (United States)