# Pro-Med Instruments Gmbh – FDA Inspection, Nov 6, 2014

Source: https://www.keypedia.com/records/fda_inspections/pro-med-instruments-gmbh/91f70049-e14c-404f-80e1-c7b5e6359744
Source feed: FDA_Inspections

> FDA inspection 905154 of Pro-Med Instruments Gmbh, November 06, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 905154
- Company Name: Pro-Med Instruments Gmbh
- Inspection Date: 2014-11-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1015579 - 2017-06-22](https://www.keypedia.com/records/fda_inspections/pro-med-instruments-gmbh/8094725e-507c-40bb-989a-e41f2bb6fdd0)
- FDA Inspection 790986 - 2012-06-21

Company: https://www.keypedia.com/companies/pro-med-instruments-gmbh/bc9526ab-268f-4f3c-82e5-f6f2b0b14394

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