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FDA Inspection
•Neuroptics Inc•May 25, 2017

Neuroptics Inc – FDA Inspection, May 25, 2017

Record Details

This FDA Inspection record concerns Neuroptics Inc, with an inspection on May 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Neuroptics Inc
Inspection Date
May 25, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Sonya L. Karsik (FDA Associated Person)
View Company Profile

ID · ac7eb9de-c21b-4e93-95c4-e22796842aab

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1017583
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Neuroptics Inc

1
DateClassificationOfficeProject area
September 12, 2018Not classifiedLos Angeles District Office
Other documents for Neuroptics Inc
  • FDA Inspection 1123593 - 2018-09-12

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