Sunright CorporationDecember 12, 2022

FDA 483 - Sunright Corporation - December 12, 2022

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Record Details

During an inspection of SUNRIGHT CORPORATION in City Of Industry, CA, the FDA observed a significant deficiency related to the firm's Foreign Supplier Verification Program (FSVP). The company failed to develop an FSVP for multiple imported food products, including Honey Flavor Syrup, Agar Ball, and Instant Mochi Powder. The importer also demonstrated unfamiliarity with FSVP requirements, indicating a lack of compliance with import regulations.

Company: Sunright Corporation
Inspection Date: December 12, 2022
Product Type: Other
Office: Division of Pharmaceutical Quality Operations IV
Person: Pamela Y. Lee (Import Specialist at U.S. Food and Drug Administration)

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ID · 19f1e800-a076-40aa-8a63-dab9f46273ef