FDA Inspection 1226106 — Instrumed International Inc

Instrumed International Inc — FEI 1421101

The FDA completed an inspection of Instrumed International Inc on December 5, 2023 in Schaumburg, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 5, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Schaumburg, IL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
320021 CFR 820.40(a)Document locations, Dissemination, etc.
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures