# FDA Inspection 920558 - Johnson & Johnson Medical GMBH - March 05, 2015

Source: https://www.keypedia.com/records/fda_inspections/johnson-johnson-medical-gmbh/07bbc9bf-67b1-4a98-bdfd-130d3ef85dc4
Source feed: FDA_Inspections

> FDA Inspection 920558 for Johnson & Johnson Medical GMBH on March 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920558
- Company Name: Johnson & Johnson Medical GMBH
- Inspection Date: 2015-03-05
- 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 920558 - 2015-03-05](https://www.keypedia.com/records/fda_inspections/johnson-johnson-medical-gmbh/43fce67e-67a0-42c6-8cb3-b341f112efae)
- [FDA Inspection 759927 - 2011-11-17](https://www.keypedia.com/records/fda_inspections/johnson-johnson-medical-gmbh/a3854387-c369-4efc-ac12-0220f4ef400b)

Company: https://www.keypedia.com/companies/johnson-johnson-medical-gmbh/c166c7e6-0d59-480b-8f15-42d000972552

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