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 2024601.
Observations2
Issue DateAugust 22, 2012
Status1 Related Warning Letter
Related Inspections3
Establishment Details
Firm
Allergan
Location
Goleta, California, United States
FEI Number
2024601
Product Type
Devices
Issue Date
August 22, 2012
Country
United States
Inspection History, 2011 to 2014
NAI2
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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