FDA Inspection 1266113 — Leltek Inc.

Leltek Inc. — FEI 3014555455

The FDA completed an inspection of Leltek Inc. on Mar 6, 2025 in New Taipei City. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 6, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
New Taipei City (Taiwan)

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