# FDA Inspection 1263062 - Intertek USA Inc. - March 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/e6965e1f-e11f-479a-9c29-88858d51ae2b
Source feed: FDA_Inspections

> FDA Inspection 1263062 for Intertek USA Inc. on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263062
- Company Name: Intertek USA Inc.
- Inspection Date: 2025-03-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: New Jersey District Office

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Company: https://www.keypedia.com/companies/intertek-usa-inc/2c61102d-28cb-4e8b-b5c0-01d3148f07d0

Office: https://www.keypedia.com/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248