FDA Inspection 985551 — Accumedix, Inc.
The FDA completed an inspection of Accumedix, Inc. on Aug 17, 2016 in Libertyville, IL. 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
- Aug 17, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Libertyville, IL (United States)