FDA Inspection 1307894 — Mytamed Inc

Mytamed Inc — FEI 3006259840

The FDA completed an inspection of Mytamed Inc on March 3, 2026 in Malvern, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 3, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Malvern, PA (United States)