FDA Inspection 1258259 — Sixarp, LLC

Sixarp, LLC — FEI 1000115322

The FDA completed an inspection of Sixarp, LLC on March 6, 2025 in Grand Rapids, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 6, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Rapids, MI (United States)