# BEKA Hospitec Gmbh – FDA Inspection, Feb 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/beka-hospitec-gmbh/77ed762b-461b-4422-b109-21ed18a04deb
Source feed: FDA_Inspections

> FDA inspection 1002323 of BEKA Hospitec Gmbh, February 02, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002323
- Company Name: BEKA Hospitec Gmbh
- Inspection Date: 2017-02-02
- 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: 8

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/beka-hospitec-gmbh/36e1b5a3-322e-4846-b8d4-19133b4a4165

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