FDA Inspection 1264928 — Philips India Limited

Philips India Limited — FEI 3010685285

The FDA completed an inspection of Philips India Limited on Feb 14, 2025 in Chakan. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Chakan (India)