# FDA Inspection 934939 - Simmank GmbH & Co KG - July 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/simmank-gmbh-co-kg/803741b2-08b3-41ee-815b-4bc107a3477c
Source feed: FDA_Inspections

> FDA Inspection 934939 for Simmank GmbH & Co KG on July 08, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 934939
- Company Name: Simmank GmbH & Co KG
- Inspection Date: 2015-07-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 934939 - 2015-07-08](https://www.keypedia.com/records/fda_inspections/simmank-gmbh-co-kg/3a59bd81-c6c8-442b-9adb-a282532e8904)

Company: https://www.keypedia.com/companies/simmank-gmbh-co-kg/b86998c5-c1d4-4414-8dca-11b2b1afcda5

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