FDA Inspection 992359 — AGP-Medical, LLC

AGP-Medical, LLC — FEI 3006145905

The FDA completed an inspection of AGP-Medical, LLC on November 8, 2016 in Suffield, CT. 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
November 8, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Suffield, CT (United States)