FDA Inspection 1192167 — Gulden Ophthalmics

Gulden Ophthalmics — FEI 2518410

The FDA completed an inspection of Gulden Ophthalmics on October 27, 2022 in Elkins Park, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 27, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkins Park, PA (United States)