FDA Inspection 1279741 — Omni Lens Private Limited

Omni Lens Private Limited — FEI 3008449456

The FDA completed an inspection of Omni Lens Private Limited on Jul 10, 2025 in Ahmedabad. 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
Jul 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Ahmedabad (India)

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