# RAUMEDIC - MUENCHBERG – FDA Inspection, Feb 2, 2023

Source: https://www.keypedia.com/records/fda_inspections/raumedic-muenchberg/499ddc9e-b4a1-49bc-837c-d2efd3b6658a
Source feed: FDA_Inspections

> FDA inspection 1196563 of RAUMEDIC - MUENCHBERG, February 02, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1196563
- Company Name: RAUMEDIC - MUENCHBERG
- Inspection Date: 2023-02-02
- 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: 2

## Related Documents

- [FDA Inspection 1031821 - 2017-11-02](https://www.keypedia.com/records/fda_inspections/raumedic-muenchberg/82c76c14-bb4a-43a9-a4ad-298c84eece88)
- [FDA Inspection 917689 - 2015-01-29](https://www.keypedia.com/records/fda_inspections/raumedic-muenchberg/e1a74c0b-e1e3-4eeb-b8a2-52b327597ad0)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/miaja-umaedi/0a41661f-08bb-4523-ab09-b17e230068e0)

Company: https://www.keypedia.com/companies/raumedic-muenchberg/88b436ec-f171-44b6-97b6-4c393ea5aad5

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