FDA Inspection
The Flex CompanyThe Flex Company – FDA Inspection, Feb 3, 2023
Record Details
This FDA Inspection record concerns The Flex Company, with an inspection on February 3, 2023, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · e7053c02-00b5-4b50-a2cb-4da3d6b8a585
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1198976
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
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.