FDA inspection

LISI MEDICAL Remmele, Inc: FDA inspection ending Jan 14, 2015

FDA inspection 910759 · No Action Indicated (NAI) · Big Lake, MN

Key facts

Inspection ID 910759
Firm LISI MEDICAL Remmele, Inc
FEI number 3009941480
Address 17701 198th Ave Nw
City Big Lake
State MN
ZIP 55309
Country United States
Fiscal year 2015
Inspection end date Jan 14, 2015
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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