# FDA Inspection 900666 - Diabetes Sentry Products - October 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/diabetes-sentry-products/e04c0550-2807-4fe7-a5de-9bbbc9137721
Source feed: FDA_Inspections

> FDA Inspection 900666 for Diabetes Sentry Products on October 22, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900666
- Company Name: Diabetes Sentry Products
- Inspection Date: 2014-10-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 900666 - 2014-10-22](https://www.keypedia.com/records/fda_inspections/diabetes-sentry-products/13828817-9100-452e-8332-ebf3f9ce1d37)

Company: https://www.keypedia.com/companies/diabetes-sentry-products/ac64d5d6-1211-40b9-994e-3ad61a64eb8f

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