FDA Inspection 652912 — Greiner Bio-One North America, Inc.
The FDA completed an inspection of Greiner Bio-One North America, Inc. on January 15, 2010 in Monroe, NC. 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
- January 15, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Monroe, NC (United States)