# FDA Inspection 927834 - Belimed AG - April 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/belimed-ag/8885dcfb-9714-40ef-bb66-82c0648b8a9e
Source feed: FDA_Inspections

> FDA Inspection 927834 for Belimed AG on April 16, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 927834
- Company Name: Belimed AG
- Inspection Date: 2015-04-16
- 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 927834 - 2015-04-16](https://www.keypedia.com/records/fda_inspections/belimed-ag/f4740a8a-0329-4ab9-83a8-292e53e00c52)
- [FDA Inspection 794094 - 2012-08-10](https://www.keypedia.com/records/fda_inspections/belimed-ag/68daeaee-f74b-43cc-a9f9-b6c452d255c6)
- [FDA Inspection 794094 - 2012-08-10](https://www.keypedia.com/records/fda_inspections/belimed-ag/0736a8d4-4cf6-44f6-a620-104af4b7d50c)

Company: https://www.keypedia.com/companies/belimed-ag/94b587fc-c8fc-4b26-af5c-06a75d7e6857

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