FDA inspection

Fresenius USA Manufacturing, Inc: FDA inspection ending Dec 7, 2022

FDA inspection 1195086 · No Action Indicated (NAI) · Knoxville, TN

Key facts

Inspection ID 1195086
Firm Fresenius USA Manufacturing, Inc
FEI number 3013546115
Address 5105 S National Dr
City Knoxville
State TN
ZIP 37914
Country United States
Fiscal year 2023
Inspection end date Dec 7, 2022
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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