FDA inspection

Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.): FDA inspection ending Feb 19, 2013

FDA inspection 816055 · No Action Indicated (NAI) · Saint Paul, MN

Key facts

Inspection ID 816055
Firm Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.)
FEI number 2183620
Address 2575 University Ave W
City Saint Paul
State MN
ZIP 55114
Country United States
Fiscal year 2013
Inspection end date Feb 19, 2013
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
  • 10–99 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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