FDA Inspection 782611 — Mesa Laboratories, Inc., Bozeman Manufacturing Facility
The FDA completed an inspection of Mesa Laboratories, Inc., Bozeman Manufacturing Facility on May 11, 2012 in Bozeman, MT. 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
- May 11, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bozeman, MT (United States)