# FDA Inspection 1198976 - The Flex Company - February 03, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/the-flex-company/e7053c02-00b5-4b50-a2cb-4da3d6b8a585
Source feed: FDA_Inspections

> FDA Inspection 1198976 for The Flex Company on February 03, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1198976
- Company Name: The Flex Company
- Inspection Date: 2023-02-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1198976 - 2023-02-03](https://www.globalkeysolutions.net/records/fda_inspections/the-flex-company/15a01add-1034-4e48-8ceb-80c38870f70d)

Company: https://www.globalkeysolutions.net/companies/the-flex-company/c36044e8-fe95-4a64-825f-8d8593f6b435

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