FDA Warning Letter — Leltek Inc.

Case 710787 — FEI 3014555455

The FDA took a Warning Letter action against Leltek Inc. on Jul 17, 2025 (New Taipei City, Taiwan). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Leltek Inc.
Date
Jul 17, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
New Taipei City (Taiwan)

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