FDA Inspection 1299818 — Medline Industries, LP

Medline Industries, LP — FEI 1417411

The FDA completed an inspection of Medline Industries, LP on Feb 6, 2026 in Arlington Heights, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
Feb 6, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Arlington Heights, IL (United States)

Citations

IDCFRDescription
23236ISO 13485:2016 Clause 8.3.1Nonconforming product not identified and controlled
23238ISO 13485:2016 Clause 8.3.1Nonconforming product not adequately evaluated