FDA Inspection
Continental Soft Lens, IncContinental Soft Lens, Inc – FDA Inspection, Oct 21, 2015
Record Details
This FDA Inspection record concerns Continental Soft Lens, Inc, with an inspection on October 21, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Continental Soft Lens, Inc
- Inspection Date
- October 21, 2015
- Product Type
- Devices
View Company Profile
ID · 52e134aa-1b93-404d-a37d-dea8dc321f83
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 950063
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Continental Soft Lens, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 24, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Continental Soft Lens, Inc
- FDA Inspection 667778 - 2010-03-24
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