FDA Inspection 1050210 — ADMI

ADMI — FEI 3010057321

The FDA completed an inspection of ADMI on Apr 17, 2018 in East Syracuse, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
East Syracuse, NY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.