FDA Inspection 1266113 — Leltek Inc.

Leltek Inc. — FEI 3014555455

The FDA completed an inspection of Leltek Inc. on March 6, 2025 in New Taipei City. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

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