# FDA Inspection 955511 - TYROMOTION GMBH - December 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/tyromotion-gmbh/f52381f4-6956-4f0c-87f5-0dc3b6769e86
Source feed: FDA_Inspections

> FDA Inspection 955511 for TYROMOTION GMBH on December 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955511
- Company Name: TYROMOTION GMBH
- Inspection Date: 2015-12-17
- 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/tyromotion-gmbh/4b6f5cd2-2bd3-46af-a132-0c57deb4d774

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