FDA Inspection 1291402 - Lightwave - October 22, 2025

Record Details

This FDA Inspection record concerns Lightwave, with an inspection on October 22, 2025, issued by the Denver District Office, covering medical devices & rad health.

Company: Lightwave
Inspection Date: October 22, 2025
Product Type: Medical Devices & Rad Health
Office: Denver District Office

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ID · cbc2c446-e7cd-4410-9cb5-fe0399908836

Violation Codes10

21 CFR 801.20(a)21 CFR 803.1721 CFR 820.100(a)21 CFR 820.12021 CFR 820.18121 CFR 820.18421 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(a)

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