# FDA Inspection 791683 - The Smartpill Corporation - July 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/the-smartpill-corporation/20e2b02e-0f36-4db6-8e77-ba1874d9b2b2
Source feed: FDA_Inspections

> FDA Inspection 791683 for The Smartpill Corporation on July 23, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791683
- Company Name: The Smartpill Corporation
- Inspection Date: 2012-07-23
- 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 791683 - 2012-07-23](https://www.keypedia.com/records/fda_inspections/the-smartpill-corporation/ad390349-63dc-4b23-9a28-fef7e192f4a4)
- [FDA Inspection 557516 - 2009-01-08](https://www.keypedia.com/records/fda_inspections/the-smartpill-corporation/7ee7f460-4426-4902-b402-9335f291a23e)
- [FDA Inspection 557516 - 2009-01-08](https://www.keypedia.com/records/fda_inspections/the-smartpill-corporation/7e01bca0-c271-4c30-9ee9-a40a26240b9e)

Company: https://www.keypedia.com/companies/the-smartpill-corporation/86d75e31-3549-4a2f-bd87-e833c8783bea

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