FDA Inspection 1013474 — Ortho-Clinical Diagnostics

Ortho-Clinical Diagnostics — FEI 1000305841

The FDA completed an inspection of Ortho-Clinical Diagnostics on March 31, 2017 in Rochester, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Rochester, NY (United States)

Citations

IDCFRDescription
1471621 CFR 820.30(f)Design verification - output does not meet input requirement