FDA Inspection 1269039 - Luminopia Inc - May 02, 2025

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Record Details

This FDA Inspection record concerns Luminopia Inc, with an inspection on May 2, 2025, issued by the New England District Office, covering medical devices & rad health.

Company: Luminopia Inc
Inspection Date: May 2, 2025
Product Type: Medical Devices & Rad Health
Office: New England District Office

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ID · e9840992-660b-4af7-94cd-08879625e777

Violation Codes1

21 CFR 820.184

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