FDA Inspection 710437 — Beckman Coulter Inc.
The FDA completed an inspection of Beckman Coulter Inc. on Feb 8, 2011 in Brea, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Feb 8, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Brea, CA (United States)