# FDA 483 - Kepix, Corp. - January 31, 2023

Source: https://www.keypedia.com/records/483/kepix-corp/f0f03dbe-9d70-4bdc-9ca9-6eaafd1a1929

> FDA 483 for Kepix, Corp. on January 31, 2023. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Kepix, Corp.
- Inspection Date: 2023-01-31
- Product Type: other
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Kepi's, Corp. in Miami, FL, revealed a significant repeat observation regarding the firm's Foreign Supplier Verification Program (FSVP). The company failed to develop an FSVP for any of the foods it imported, a deficiency noted in multiple previous inspections. This indicates a persistent issue with compliance related to imported food safety regulations.

## Related Officers

- [Laura M. Lopez](https://www.keypedia.com/people/laura-m-lopez/5c971465-15dc-4971-a1ac-1edfc3cb5ab7)

Company: https://www.keypedia.com/companies/kepix-corp/60ed7fa5-9d9e-4ee5-b9c0-18153f03ef99

Office: https://www.keypedia.com/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6
