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FDA Inspection 984848 — Medline Industries, LP

Medline Industries, LP — FEI 1417592

The FDA completed an inspection of Medline Industries, LP on May 26, 2016 in Northfield, 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
May 26, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northfield, IL (United States)

Facility

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  • 1166522 (NAI Wed Apr 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 822017 (NAI Wed Mar 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 706656 (NAI Fri Jan 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 652020 (NAI Mon Mar 08 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources