FDA Inspection 1320398 — Acero Precision

Acero Precision — FEI 3000170817

The FDA completed an inspection of Acero Precision on May 8, 2026 in West Chester, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 8, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, PA (United States)