483
Stepan CompanyFDA 483 - Stepan Company - March 04, 2022
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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.
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