# FDA Inspection 1020846 - Pro Med Instruments GMBH - June 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/pro-med-instruments-gmbh/9ade7960-f5d6-4455-b883-c9aec9613f04
Source feed: FDA_Inspections

> FDA Inspection 1020846 for Pro Med Instruments GMBH on June 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020846
- Company Name: Pro Med Instruments GMBH
- Inspection Date: 2017-06-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/pro-med-instruments-gmbh/d7c7b3c3-8283-45aa-af6a-f2da6ece5458

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