# FDA Inspection 1059835 - BEMA-GMBH & CO. KG - July 19, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/bema-gmbh-co-kg/d6c7b6db-ecd6-4a18-9711-5e52bc83aa11
Source feed: FDA_Inspections

> FDA Inspection 1059835 for BEMA-GMBH & CO. KG on July 19, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059835
- Company Name: BEMA-GMBH & CO. KG
- Inspection Date: 2018-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1059835 - 2018-07-19](https://www.globalkeysolutions.net/records/fda_inspections/bema-gmbh-co-kg/79e10465-d3f6-4b84-b6af-49d8a8e88c00)

Company: https://www.globalkeysolutions.net/companies/bema-gmbh-co-kg/ac4ef033-ea21-4141-86ac-c99cb6c87c98

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