# FDA Inspection 991500 - Radiometer Basel AG - October 20, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/radiometer-basel-ag/a25c9884-6d73-4a97-b555-84b8f362cb82/
Source feed: FDA_Inspections

> FDA Inspection 991500 for Radiometer Basel AG on October 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991500
- Company Name: Radiometer Basel AG
- Inspection Date: 2016-10-20
- 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 991500 - 2016-10-20](https://www.globalkeysolutions.net/api/records/fda_inspections/radiometer-basel-ag/f744b06f-930c-4da2-bcf1-272b49b2709f/)
- [FDA Inspection 575847 - 2009-03-26](https://www.globalkeysolutions.net/api/records/fda_inspections/radiometer-basel-ag/66588f76-8071-497b-a8ba-606133965cb9/)

Company: https://www.globalkeysolutions.net/companies/radiometer-basel-ag/4c0d1b05-e674-4961-bf6b-9f97ee873689

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