FDA Inspection 668729 — Sixarp, LLC

Sixarp, LLC — FEI 1000115322

The FDA completed an inspection of Sixarp, LLC on May 28, 2010 in Grand Rapids, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 28, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Rapids, MI (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
436821 CFR 211.188(b)(12)Investigations made into any unexplained discrepancy

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