FDA inspection

Lake Region Manufacturing, Inc: FDA inspection ending Feb 2, 2005

FDA inspection 364844 · No Action Indicated (NAI) · Chaska, MN

Key facts

Inspection ID 364844
Firm Lake Region Manufacturing, Inc
FEI number 2126666
Address 340 Lake Hazeltine Dr
City Chaska
State MN
ZIP 55318-1034
Fiscal year 2005
Inspection end date Feb 2, 2005
Classification No Action Indicated (NAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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