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FDA Inspection 1102731 — Ortho Solutions LC

Ortho Solutions LC — FEI 1937100

The FDA completed an inspection of Ortho Solutions LC on September 5, 2019 in Lake Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lake Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 1218587 (NAI Mon Sep 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1048804 (NAI Wed Apr 18 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources