# The Flex Company – FDA Inspection, Feb 3, 2023

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

> FDA inspection 1198976 of The Flex Company, February 03, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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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)
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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

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