FDA Inspection 1221713 — Agiliti Health - Ellis

Agiliti Health - Ellis — FEI 3002693132

The FDA completed an inspection of Agiliti Health - Ellis on November 2, 2023 in Ellis, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 2, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ellis, KS (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures