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FDA Inspection 1048804 — Ortho Solutions LC

Ortho Solutions LC — FEI 1937100

The FDA completed an inspection of Ortho Solutions LC on April 18, 2018 in Lake Saint Louis, MO. 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
April 18, 2018
Fiscal Year
2018
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))
  • 1102731 (VAI Thu Sep 05 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources