FDA inspection

Sunrich Products, LLC: FDA inspection ending Oct 18, 2010

FDA inspection 685521 · No Action Indicated (NAI) · Breckenridge, MN

Key facts

Inspection ID 685521
Firm Sunrich Products, LLC
FEI number 1717077
Address 1971 354th St
City Breckenridge
State MN
ZIP 56520
Country United States
Fiscal year 2011
Inspection end date Oct 18, 2010
Classification No Action Indicated (NAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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