FDA Inspection 1229069 — Katecho LLC

Katecho LLC — FEI 1930027

The FDA completed an inspection of Katecho LLC on August 1, 2024 in Des Moines, IA. 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
August 1, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Des Moines, IA (United States)