# Flex-Cell Precision, Inc – FDA Inspection, Feb 3, 2023

Source: https://www.keypedia.com/records/fda_inspections/flex-cell-precision-inc/f135601c-4cf8-40c4-9df4-c105d0c18973
Source feed: FDA_Inspections

> FDA inspection 1196722 of Flex-Cell Precision, Inc, February 03, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1196722
- Company Name: Flex-Cell Precision, Inc
- Inspection Date: 2023-02-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1089368 - 2019-03-27](https://www.keypedia.com/records/fda_inspections/flex-cell-precision-inc/ff270666-13f9-4a4b-9f3e-6f877fc8d7c5)

## Related Officers

- [Investigator](https://www.keypedia.com/people/nadia-r-barreda/ef624359-957a-45e4-89c9-5b5ff215c6aa)

Company: https://www.keypedia.com/companies/flex-cell-precision-inc/95877302-41b0-4e88-a33d-44901b72e805

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7