Vitrolife Inc.January 23, 2025

FDA 483 - Vitrolife Inc. - January 23, 2025

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Vitrolife Inc. in San Diego, CA, was inspected from January 21-23, 2025, and received one observation. The firm was cited for inadequate complaint handling, specifically regarding its procedures lacking investigation requirements for device failures and the failure to investigate a complaint about a "lint-like a hair" in a sterilized Biopsy Pipette package.

Company: Vitrolife Inc.
Inspection Date: January 23, 2025
Product Type: Device
Office: Los Angeles District Office
Person: Juanj Wu

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ID · 5c2c60ef-506c-4850-ba06-09c277d5225d