FDA Inspection 893426 — Medela Inc

Medela Inc — FEI 1419937

The FDA completed an inspection of Medela Inc on August 27, 2014 in Mchenry, IL. 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
August 27, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Mchenry, IL (United States)