FDA Inspection 1181164 — Katecho LLC

Katecho LLC — FEI 1930027

The FDA completed an inspection of Katecho LLC on September 15, 2022 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
September 15, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Des Moines, IA (United States)

Additional Details

Postmarket Audit Inspections