FDA Inspection 1293588 — Henry Schein Inc.

Henry Schein Inc. — FEI 1000143438

The FDA completed an inspection of Henry Schein Inc. on September 22, 2025 in Denver, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 22, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Denver, PA (United States)