# FDA Inspection 879680 - Invivo Germany Gmbh - April 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/invivo-germany-gmbh/b933727e-e69c-4d64-bd62-6878abd9bb62
Source feed: FDA_Inspections

> FDA Inspection 879680 for Invivo Germany Gmbh on April 24, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 879680
- Company Name: Invivo Germany Gmbh
- Inspection Date: 2014-04-24
- 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 879680 - 2014-04-24](https://www.keypedia.com/records/fda_inspections/invivo-germany-gmbh/152a3dda-5d93-435f-8d79-a550382f2b71)

Company: https://www.keypedia.com/companies/invivo-germany-gmbh/bc34038b-de52-412f-8f72-bc02249b16a5

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