FDA Inspection 1050210 — ADMI

ADMI — FEI 3010057321

The FDA completed an inspection of ADMI on April 17, 2018 in East Syracuse, NY. 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
April 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
East Syracuse, NY (United States)