FDA Inspection 682946 — Fresenius Kabi USA LLC (FK USA)

Fresenius Kabi USA LLC (FK USA) — FEI 3007344667

The FDA completed an inspection of Fresenius Kabi USA LLC (FK USA) on Sep 17, 2010 in Bensenville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 17, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bensenville, IL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures