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 3003515967.
Observations1
Issue DateDecember 19, 2024
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Menicon America, Inc.
Location
North Billerica, Massachusetts, United States
FEI Number
3003515967
Product Type
Devices
Issue Date
December 19, 2024
Country
United States
Inspection History, 2015 to 2024
NAI2
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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