# FDA 483 - Sunright Corporation - December 12, 2022

Source: https://www.globalkeysolutions.net/records/483/sunright-corporation/19f1e800-a076-40aa-8a63-dab9f46273ef

> FDA 483 for Sunright Corporation on December 12, 2022. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Sunright Corporation
- Inspection Date: 2022-12-12
- Product Type: other
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: 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.

## Related Officers

- [Import Specialist at U.S. Food and Drug Administration](https://www.globalkeysolutions.net/people/pamela-y-lee/e632ec32-0808-44ae-b6a1-6fe6b3c93528)

Company: https://www.globalkeysolutions.net/companies/sunright-corporation/eca5d72c-3b98-441e-87b0-94e28bbb3188

Office: https://www.globalkeysolutions.net/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6