FDA Inspection 1283240 — Myron L Company

Myron L Company — FEI 2020976

The FDA completed an inspection of Myron L Company on September 19, 2025 in Carlsbad, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 19, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Carlsbad, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures