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483
•Sol-ti, Inc.•February 8, 2023

Sol-ti, Inc. – FDA 483, Feb 8, 2023

Record Details

Sol-ti Inc. in San Diego, CA, a juice manufacturer, was cited for significant deficiencies in its HACCP plan validation, hazard analysis, monitoring procedures, and sanitation practices for juice products. Additionally, the inspection revealed a lack of established quality control procedures, component and finished product specifications, and proper manufacturing records for its dietary supplement products. These issues indicate a broad failure to adhere to good manufacturing practices and ensure product safety and quality.

Company
Sol-ti, Inc.
Inspection date
February 8, 2023
Product type
other
Office
Division of Pharmaceutical Quality Operations IV
People
  • Mary C. Wall
  • Sparky L Bartee
View Company Profile

ID · b5605743-51f9-4830-95d8-86bf4c6d2004

Other documents for Sol-ti, Inc.
  • 483 - 2023-10-05October 5, 2023
  • WARNING_LETTER - 2023-02-08February 8, 2023

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