FDA inspection

Sterilmed, Inc.: FDA inspection ending Jun 22, 2018

FDA inspection 1058879 · No Action Indicated (NAI) · Plymouth, MN

Key facts

Inspection ID 1058879
Firm Sterilmed, Inc.
FEI number 3011276773
Address 5010 Cheshire Pkwy N Ste 2
City Plymouth
State MN
ZIP 55446
Country United States
Fiscal year 2018
Inspection end date Jun 22, 2018
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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