FDA inspection

Lake Region Manufacturing, Inc: FDA inspection ending Jun 2, 2016

FDA inspection 977543 · No Action Indicated (NAI) · Chaska, MN

Key facts

Inspection ID 977543
Firm Lake Region Manufacturing, Inc
FEI number 2126666
Address 340 Lake Hazeltine Dr
City Chaska
State MN
ZIP 55318
Country United States
Fiscal year 2016
Inspection end date Jun 2, 2016
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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