# HIDREX GmbH – FDA Inspection, Nov 9, 2023

Source: https://www.keypedia.com/records/fda_inspections/hidrex-gmbh/70cfdecc-fa00-4bb0-b38e-5e273f72cda8
Source feed: FDA_Inspections

> FDA inspection 1222347 of HIDREX GmbH, November 09, 2023. Classification: Official Action Indicated (OAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222347
- Company Name: HIDREX GmbH
- Inspection Date: 2023-11-09
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1002806 - 2017-01-26](https://www.keypedia.com/records/fda_inspections/hidrex-gmbh/a67611a9-bd04-43e9-885a-ed565f3aa4be)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

Company: https://www.keypedia.com/companies/hidrex-gmbh/eeb8238b-2324-4f56-bf8c-600717ff2e64

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