# FDA Inspection 783942 - EyeTel Imaging, Inc. - May 22, 2012

Source: https://www.keypedia.com/records/fda_inspections/eyetel-imaging-inc/e4c28d10-2f51-40cc-a487-c014075e73ac
Source feed: FDA_Inspections

> FDA Inspection 783942 for EyeTel Imaging, Inc. on May 22, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783942
- Company Name: EyeTel Imaging, Inc.
- Inspection Date: 2012-05-22
- 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 783942 - 2012-05-22](https://www.keypedia.com/records/fda_inspections/eyetel-imaging-inc/b04b7849-2c36-43cf-a2c4-08ce4cfd3019)
- [FDA Inspection 560403 - 2009-01-27](https://www.keypedia.com/records/fda_inspections/eyetel-imaging-inc/4cf82c56-1344-471e-8584-2ac28cf785c9)

Company: https://www.keypedia.com/companies/eyetel-imaging-inc/27dac0f4-af38-4b68-8ad0-d7fa7b25bf7e

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