FDA inspection

Sixarp, LLC: FDA inspection ending Feb 15, 2012

FDA inspection 780535 · No Action Indicated (NAI) · Grand Rapids, MI

Key facts

Inspection ID 780535
Firm Sixarp, LLC
FEI number 1000115322
Address 7650 Caterpillar Ct Sw Ste D
City Grand Rapids
State MI
ZIP 49548-7206
Fiscal year 2012
Inspection end date Feb 15, 2012
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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