FDA Inspection 1218976 — Interplex Medical LLC

Interplex Medical LLC — FEI 3005221616

The FDA completed an inspection of Interplex Medical LLC on September 20, 2023 in Milford, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Milford, OH (United States)