FDA Inspection 1169813 — Lenstec (Barbados) Inc.

Lenstec (Barbados) Inc. — FEI 3001284430

The FDA completed an inspection of Lenstec (Barbados) Inc. on Apr 22, 2022 in Christ Church. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 22, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Christ Church (Barbados)

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