# FDA Inspection 950063 - Continental Soft Lens, Inc - October 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/continental-soft-lens-inc/52e134aa-1b93-404d-a37d-dea8dc321f83
Source feed: FDA_Inspections

> FDA Inspection 950063 for Continental Soft Lens, Inc on October 21, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950063
- Company Name: Continental Soft Lens, Inc
- Inspection Date: 2015-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 950063 - 2015-10-21](https://www.keypedia.com/records/fda_inspections/continental-soft-lens-inc/480ccdb3-ce2e-424b-b134-4287cc05cbbe)
- [FDA Inspection 667778 - 2010-03-24](https://www.keypedia.com/records/fda_inspections/continental-soft-lens-inc/098a4d61-7504-419b-bebf-501b1673dad8)

Company: https://www.keypedia.com/companies/continental-soft-lens-inc/e10cb46e-bbf1-4c95-9dcd-89ddb651cdc5

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