Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2518410.
Observations4
Issue DateJanuary 27, 2010
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Gulden Ophthalmics
Location
Elkins Park, Pennsylvania, United States
FEI Number
2518410
Product Type
Devices
Issue Date
January 27, 2010
Country
United States
Inspection History, 2010 to 2022
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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