# FDA Inspection 916161 - Radiometer America Inc - March 02, 2015

Source: https://www.keypedia.com/records/fda_inspections/radiometer-america-inc/c8faadb3-e6e6-4a4d-aef3-fb51651f7c62
Source feed: FDA_Inspections

> FDA Inspection 916161 for Radiometer America Inc on March 02, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916161
- Company Name: Radiometer America Inc
- Inspection Date: 2015-03-02
- 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 916161 - 2015-03-02](https://www.keypedia.com/records/fda_inspections/radiometer-america-inc/c00b1043-0f03-4982-9e98-49c1ac21f4ba)
- [FDA Inspection 740585 - 2011-08-18](https://www.keypedia.com/records/fda_inspections/radiometer-america-inc/5c57d4e5-9e3c-4694-beb2-dd2535745b2a)
- [FDA Inspection 740585 - 2011-08-18](https://www.keypedia.com/records/fda_inspections/radiometer-america-inc/963ce140-d4a6-4f12-8c28-c5ae48a00edd)

Company: https://www.keypedia.com/companies/radiometer-america-inc/7b5ff45b-7a35-4ec2-8a04-7073f148ca09

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