FDA Inspection 1294096 — Sixarp, LLC

Sixarp, LLC — FEI 3032422332

The FDA completed an inspection of Sixarp, LLC on November 19, 2025 in Byron Center, 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
November 19, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Byron Center, MI (United States)