# FDA Inspection 976542 - VisionAid, Inc. - July 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/visionaid-inc/067b2642-4153-441a-823c-61c4f825e208
Source feed: FDA_Inspections

> FDA Inspection 976542 for VisionAid, Inc. on July 12, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976542
- Company Name: VisionAid, Inc.
- Inspection Date: 2016-07-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 764065 - 2012-01-20](https://www.keypedia.com/records/fda_inspections/visionaid-inc/2399aff4-2d84-4757-88e0-b393a0fb52d4)
- [FDA Inspection 764065 - 2012-01-20](https://www.keypedia.com/records/fda_inspections/visionaid-inc/ef8ff59c-fa32-462a-a032-1e49de52e7c8)
- [FDA Inspection 631983 - 2009-12-02](https://www.keypedia.com/records/fda_inspections/visionaid-inc/f1797941-48b7-4175-ade2-37f9df4e0922)

Company: https://www.keypedia.com/companies/visionaid-inc/4acdf323-2f7c-4fa1-8567-8f0f0a1f69f2

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