# FDA Inspection 1008014 - Ackermann Instrumente Gmbh - March 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/ackermann-instrumente-gmbh/9566d998-8e02-4dd3-9d8b-4da7a224bb02
Source feed: FDA_Inspections

> FDA Inspection 1008014 for Ackermann Instrumente Gmbh on March 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008014
- Company Name: Ackermann Instrumente Gmbh
- Inspection Date: 2017-03-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1008014 - 2017-03-08](https://www.keypedia.com/records/fda_inspections/ackermann-instrumente-gmbh/5787d07a-e957-4a0e-a128-9d1572872597)

Company: https://www.keypedia.com/companies/ackermann-instrumente-gmbh/dce397f8-e0f7-4c65-8767-d5436e170a03

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