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483
•Stepan Company•March 4, 2022

Stepan Company – FDA 483, Mar 4, 2022

Record Details

During an inspection of Stepan Company in Northfield, IL, the FDA observed a significant deficiency in the firm's Foreign Supplier Verification Program. The company failed to develop an FSVP plan for imported food ingredients, specifically Clarinol G-80 and Clarinol Powder. This indicates a lack of compliance with fundamental regulatory requirements for ensuring the safety of imported foods.

Company
Stepan Company
Inspection date
March 4, 2022
Product type
other
Office
Chicago District Office
Person
  • Nicholas J. Presto
View Company Profile

ID · 2f0b7661-2006-43c7-b1ac-71dc8c4bd232

Other documents for Stepan Company
  • EIR - 2022-03-04March 4, 2022

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