FDA Inspection
Mesa Laboratories, Inc.Mesa Laboratories, Inc. – FDA Inspection, Mar 16, 2018
Record Details
This FDA Inspection record concerns Mesa Laboratories, Inc., with an inspection on March 16, 2018, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 72dd0034-fdc4-4635-992b-8f5aa98d7680
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1044777
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.200(a)Servicing - Lack of or inadequate procedures
- 21 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Mesa Laboratories, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 5, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mesa Laboratories, Inc.
- FDA Inspection 917352 - 2015-03-05
- FDA Inspection 796546 - 2012-08-29
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.