FDA Inspection 1279557 - Eurofins Lancaster Laboratories, Inc - August 26, 2025
FDA Inspection 1279557 for Eurofins Lancaster Laboratories, Inc on August 26, 2025. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 1279557 for Eurofins Lancaster Laboratories, Inc on August 26, 2025. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
August 26, 2025
Product Type
Drugs
ID: 5f51c7f6-0053-45a3-b706-74ebfcd5cb8b
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