# BEMA-GMBH & CO. KG – FDA Inspection, Jul 19, 2018

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

> FDA inspection 1059835 of BEMA-GMBH & CO. KG, July 19, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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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)
- 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 Officers

- Issuing Officer

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

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