FDA Inspection 1020265 — Biomerieux, Inc.
The FDA completed an inspection of Biomerieux, Inc. on July 27, 2017 in Lombard, 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
- July 27, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lombard, IL (United States)