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483
•Domico Med-Device Llc•May 12, 2026

Domico Med-Device Llc – FDA 483, May 12, 2026

Record Details

During an inspection, Domico Med-Device Llc in Fenton, MI, was cited for significant deficiencies across its quality system. Observations included inadequate risk management documentation, insufficient equipment calibration justifications, and gaps in complaint handling procedures. The firm also lacked proper qualification for production infrastructure and had deficiencies in its corrective and preventive action system, indicating a broad need for quality system improvements.

Company
Domico Med-Device Llc
Inspection date
May 12, 2026
Product type
device
Office
Division of Pharmaceutical Quality Operations III
Person
  • Felicia E. Armbrustmacher (investigator)
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ID · 6c630ba4-24b2-45bc-9fd8-fc0a93eda9d6

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