FDA Inspection 1260503 — Incoba LLC

Incoba LLC — FEI 3017865349

The FDA completed an inspection of Incoba LLC on Feb 4, 2025 in Chesterfield, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 4, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chesterfield, MO (United States)