Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3010882984.
Observations2
Issue DateFebruary 12, 2026
StatusNo Warning Letter
Establishment TypeContract Manufacturer
Related Inspections4
Establishment Details
Firm
Therapak Corporation
Location
Claremont, California
FEI Number
3010882984
Establishment Type
Contract Manufacturer
Product Type
Devices
Issue Date
February 12, 2026
Country
United States
Inspection History, 2010 to 2026
NAI3
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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