# Flex-Cell Precision, Inc – FDA Inspection, Mar 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/flex-cell-precision-inc/ff270666-13f9-4a4b-9f3e-6f877fc8d7c5
Source feed: FDA_Inspections

> FDA inspection 1089368 of Flex-Cell Precision, Inc, March 27, 2019. Classification: Voluntary Action Indicated (VAI). 5 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: 1089368
- Company Name: Flex-Cell Precision, Inc
- Inspection Date: 2019-03-27
- 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: 5

## Related Documents

- [FDA Inspection 1196722 - 2023-02-03](https://www.keypedia.com/records/fda_inspections/flex-cell-precision-inc/f135601c-4cf8-40c4-9df4-c105d0c18973)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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