FDA Inspection 1305824 - DynaFlex - March 06, 2026

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Record Details

This FDA Inspection record concerns DynaFlex, with an inspection on March 6, 2026, issued by the Kansas City District Office, covering medical devices & rad health.

Company: DynaFlex
Inspection Date: March 6, 2026
Product Type: Medical Devices & Rad Health
Office: Kansas City District Office

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ID · 9f9a3483-b6d0-4be9-a38f-109970e27856

Violation Codes5

21 CFR 801.20(a)21 CFR 803.50(a)(1)ISO 13485:2016 Clause 7.5.6ISO 13485:2016 Clause 8.2.2ISO 13485:2016 Clause 8.3.1

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