# FDA Inspection 1059152 - Blanchard Contact Lens, Inc. - July 09, 2018

Source: https://www.keypedia.com/records/fda_inspections/blanchard-contact-lens-inc/6f13140f-ef86-4769-a98e-c362bbd0ec70
Source feed: FDA_Inspections

> FDA Inspection 1059152 for Blanchard Contact Lens, Inc. on July 09, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059152
- Company Name: Blanchard Contact Lens, Inc.
- Inspection Date: 2018-07-09
- 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 1059152 - 2018-07-09](https://www.keypedia.com/records/fda_inspections/blanchard-contact-lens-inc/3be47eb6-d507-4e42-852e-8930a01ff957)
- [FDA Inspection 942180 - 2015-08-25](https://www.keypedia.com/records/fda_inspections/blanchard-contact-lens-inc/02e50450-7dab-4753-8a48-592819a04492)
- [FDA Inspection 835044 - 2013-06-10](https://www.keypedia.com/records/fda_inspections/blanchard-contact-lens-inc/9814d695-8879-4940-b9fa-d6ca293245d7)
- [FDA Inspection 735224 - 2011-06-15](https://www.keypedia.com/records/fda_inspections/blanchard-contact-lens-inc/c7fabbc9-33ab-4852-973e-0a65054c111f)

Company: https://www.keypedia.com/companies/blanchard-contact-lens-inc/472424f6-fd57-49fd-b5b1-4e2c0edfa61a

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