# FDA Inspection 790986 - Pro-Med Instruments Gmbh - June 21, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/pro-med-instruments-gmbh/82087b31-7db7-4b6e-9a10-630141281767
Source feed: FDA_Inspections

> FDA Inspection 790986 for Pro-Med Instruments Gmbh on June 21, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 790986
- Company Name: Pro-Med Instruments Gmbh
- Inspection Date: 2012-06-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 905154 - 2014-11-06](https://www.globalkeysolutions.net/records/fda_inspections/pro-med-instruments-gmbh/78290be9-3d62-481c-acba-5251a485b085)
- [FDA Inspection 905154 - 2014-11-06](https://www.globalkeysolutions.net/records/fda_inspections/pro-med-instruments-gmbh/91f70049-e14c-404f-80e1-c7b5e6359744)
- [FDA Inspection 790986 - 2012-06-21](https://www.globalkeysolutions.net/records/fda_inspections/pro-med-instruments-gmbh/4bea29fc-5c41-416b-8901-1ab387706d10)

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

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