# FDA Inspection 1089368 - Flex-Cell Precision, Inc - March 27, 2019

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

> FDA Inspection 1089368 for Flex-Cell Precision, Inc on March 27, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1089368
- Company Name: Flex-Cell Precision, Inc
- Inspection Date: 2019-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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

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

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