# FDA Inspection 838960 - Visioncare Devices, Inc. - June 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/visioncare-devices-inc/162bf9fb-b665-4eb1-8913-e202a4ded9b3
Source feed: FDA_Inspections

> FDA Inspection 838960 for Visioncare Devices, Inc. on June 26, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838960
- Company Name: Visioncare Devices, Inc.
- Inspection Date: 2013-06-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 990226 - 2016-11-03](https://www.keypedia.com/records/fda_inspections/visioncare-devices-inc/02b332ea-373a-41c4-9fd9-c3a3c68afa97)
- [FDA Inspection 990226 - 2016-11-03](https://www.keypedia.com/records/fda_inspections/visioncare-devices-inc/82db6e82-4856-41c2-a7ad-45285ef81a9c)
- [FDA Inspection 838960 - 2013-06-26](https://www.keypedia.com/records/fda_inspections/visioncare-devices-inc/4540bbdb-312a-4c7c-b941-3f02c147a43e)

Company: https://www.keypedia.com/companies/visioncare-devices-inc/d9ad0378-b32a-4a92-bf36-4a9078db5117

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