FDA Inspection 1065416 — Molnlycke Manufacturing US, Llc

Molnlycke Manufacturing US, Llc — FEI 3000719717

The FDA completed an inspection of Molnlycke Manufacturing US, Llc on Aug 30, 2018 in Wiscasset, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 30, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Wiscasset, ME (United States)