# FDA Inspection 1004476 - MediMet GmbH - February 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/medimet-gmbh/6e92511a-2fae-4ccf-ab8a-f39df057bf69
Source feed: FDA_Inspections

> FDA Inspection 1004476 for MediMet GmbH on February 15, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004476
- Company Name: MediMet GmbH
- Inspection Date: 2017-02-15
- 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 1004476 - 2017-02-15](https://www.keypedia.com/records/fda_inspections/medimet-gmbh/6509d681-c0b0-4802-9423-a6a7e7fcc5c7)

Company: https://www.keypedia.com/companies/medimet-gmbh/37d753f7-bc73-410f-b59f-f3d39e9a41ea

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