FDA Inspection 846362 — Accumedix, Inc.

Accumedix, Inc. — FEI 3003473212

The FDA completed an inspection of Accumedix, Inc. on August 6, 2013 in Libertyville, IL. 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
August 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Libertyville, IL (United States)