FDA inspection

Refractec LLC: FDA inspection ending Jun 17, 2010

FDA inspection 672612 · No Action Indicated (NAI) · Bloomington, MN

Key facts

Inspection ID 672612
Firm Refractec LLC
FEI number 3003804564
Address 5775 W Old Shakopee Rd
City Bloomington
State MN
ZIP 55437
Country United States
Fiscal year 2010
Inspection end date Jun 17, 2010
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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