FDA Inspection
Mesa Laboratories, Inc., Bozeman Manufacturing FacilityMesa Laboratories, Inc., Bozeman Manufacturing Facility – FDA Inspection, Dec 7, 2016
Record Details
This FDA Inspection record concerns Mesa Laboratories, Inc., Bozeman Manufacturing Facility, with an inspection on December 7, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 7, 2016
- Product Type
- Devices
- People
- Eric C. Fox (Investigator)
- Mary K. Concannon (Issuing Officer)
View Company Profile
ID · fd9ec0e1-8561-4885-a8b1-f510470e5f76
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1035440
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Mesa Laboratories, Inc., Bozeman Manufacturing Facility
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 23, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 14, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 14, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 20, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 11, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mesa Laboratories, Inc., Bozeman Manufacturing Facility
- FDA Inspection 1339850 - 2026-09-23
- FDA Inspection 1095806 - 2019-06-14
- FDA Inspection 926278 - 2015-05-14
- FDA Inspection 799635 - 2012-09-20
- FDA Inspection 782611 - 2012-05-11
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