FDA inspection

Fresenius Kabi USA, LLC: FDA inspection ending Mar 18, 2022

FDA inspection 1164862 · Voluntary Action Indicated (VAI) · North Andover, MA

Key facts

Inspection ID 1164862
Firm Fresenius Kabi USA, LLC
FEI number 3014732157
Address 50 High St Ste 50
City North Andover
State MA
ZIP 01845
Country United States
Fiscal year 2022
Inspection end date Mar 18, 2022
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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