# FDA Inspection 921478 - Stork Instrumente GmbH - February 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/stork-instrumente-gmbh/812ccef9-9f4a-4d83-b92b-5d204823a7e7
Source feed: FDA_Inspections

> FDA Inspection 921478 for Stork Instrumente GmbH on February 25, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 921478
- Company Name: Stork Instrumente GmbH
- Inspection Date: 2015-02-25
- 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 921478 - 2015-02-25](https://www.keypedia.com/records/fda_inspections/stork-instrumente-gmbh/80b55831-3153-4529-b97a-44b266eddde3)

Company: https://www.keypedia.com/companies/stork-instrumente-gmbh/fb6214ff-61b2-48c8-94e1-5f44a5f546c0

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