FDA Inspection
Flex-Cell Precision, IncFlex-Cell Precision, Inc – FDA Inspection, Feb 3, 2023
Record Details
This FDA Inspection record concerns Flex-Cell Precision, Inc, with an inspection on February 3, 2023, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · f135601c-4cf8-40c4-9df4-c105d0c18973
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1196722
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.22Quality audits - auditor independence
- 21 CFR 820.22Quality audits - auditor independence
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Flex-Cell Precision, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 27, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Flex-Cell Precision, Inc
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.