# FDA Inspection 699317 - DRG Instruments GmbH - October 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/drg-instruments-gmbh/aeb43609-9ec6-496d-bec1-18c0836e686f
Source feed: FDA_Inspections

> FDA Inspection 699317 for DRG Instruments GmbH on October 21, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 699317
- Company Name: DRG Instruments GmbH
- Inspection Date: 2010-10-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/drg-instruments-gmbh/5a8981ef-7bb3-4af6-a73f-01be1234ce51

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