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FDA Inspection
•Mi Gwang Contact Lens Co., Ltd.•March 8, 2018

Mi Gwang Contact Lens Co., Ltd. – FDA Inspection, Mar 8, 2018

Record Details

This FDA Inspection record concerns Mi Gwang Contact Lens Co., Ltd., with an inspection on March 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Mi Gwang Contact Lens Co., Ltd.
Inspection Date
March 8, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Thai T. Duong (Issuing Officer)
View Company Profile

ID · 9e604195-8dc4-4a02-82d1-e41b123a9dfe

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1047085
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Mi Gwang Contact Lens Co., Ltd.

3
DateClassificationOfficeProject area
December 15, 2022VAICenter for Devices and Radiological HealthCompliance: Devices
March 19, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
July 5, 2012OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Mi Gwang Contact Lens Co., Ltd.
  • FDA Inspection 1193124 - 2022-12-15
  • FDA Inspection 929308 - 2015-03-19
  • FDA Inspection 790547 - 2012-07-05

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