# ROWEMED AG – FDA Inspection, Jun 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/rowemed-ag/39551b1c-a467-4da7-b0c7-af83cd3fd992
Source feed: FDA_Inspections

> FDA inspection 1016928 of ROWEMED AG, June 22, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016928
- Company Name: ROWEMED AG
- Inspection Date: 2017-06-22
- 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: 3

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

Company: https://www.keypedia.com/companies/rowemed-ag/93982cbc-4886-4a7a-ae25-8f3157934275

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