# FDA Inspection 1023889 - Art Optical Contact Lens, Inc. - August 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/art-optical-contact-lens-inc/6f3af9cc-842a-413f-b376-2d4f50769c92
Source feed: FDA_Inspections

> FDA Inspection 1023889 for Art Optical Contact Lens, Inc. on August 30, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023889
- Company Name: Art Optical Contact Lens, Inc.
- Inspection Date: 2017-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023889 - 2017-08-30](https://www.keypedia.com/records/fda_inspections/art-optical-contact-lens-inc/42c1a011-339e-4517-8f21-490565925673)
- [FDA Inspection 761852 - 2011-12-12](https://www.keypedia.com/records/fda_inspections/art-optical-contact-lens-inc/d45ac484-575c-4d7e-8154-d599eceb0f02)
- [FDA Inspection 636358 - 2009-12-31](https://www.keypedia.com/records/fda_inspections/art-optical-contact-lens-inc/282bfff5-5e15-4f8f-82af-44f0f3cb7b2e)

Company: https://www.keypedia.com/companies/art-optical-contact-lens-inc/2ee9dd51-093b-4f93-9bb5-ff045b5c4433

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