# Continental Soft Lens, Inc – FDA Inspection, Oct 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 of Continental Soft Lens, Inc, October 21, 2015. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 667778 - 2010-03-24

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