FDA Inspection 1292506 — Lutech Industries

Lutech Industries — FEI 3036423383

The FDA completed an inspection of Lutech Industries on Oct 24, 2025 in Indianapolis, IN. 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
Oct 24, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Indianapolis, IN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.