# FDA Inspection 966726 - ALR Technologies, Inc. - March 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/alr-technologies-inc/a2ef571d-115b-4446-b42d-f6ab403d0217
Source feed: FDA_Inspections

> FDA Inspection 966726 for ALR Technologies, Inc. on March 22, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 966726
- Company Name: ALR Technologies, Inc.
- Inspection Date: 2016-03-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 844663 - 2013-08-15](https://www.keypedia.com/records/fda_inspections/alr-technologies-inc/8fa9002f-ca81-4868-8632-f7887f040ea9)

Company: https://www.keypedia.com/companies/alr-technologies-inc/6f48bdb7-01c4-4a2f-abe7-16cbb1f8c8ae

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