# FDA Inspection 886388 - Medi-Plus Instrumente Gmbh & Co. - April 03, 2014

Source: https://www.keypedia.com/records/fda_inspections/medi-plus-instrumente-gmbh-co/ea7b9a45-dbbe-4d71-bfcc-627aaa87d719
Source feed: FDA_Inspections

> FDA Inspection 886388 for Medi-Plus Instrumente Gmbh & Co. on April 03, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 886388
- Company Name: Medi-Plus Instrumente Gmbh & Co.
- Inspection Date: 2014-04-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/medi-plus-instrumente-gmbh-co/2cef63eb-216f-4194-bae3-0a8882db50f9

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