Aarti Pharmalabs Receives US FDA Inspection Report for Unit-IV

Aarti Pharmalabs Receives US FDA Inspection Report for Unit-IV

Aarti Pharmalabs Receives US FDA Inspection Report for Unit-IV​

Aarti Pharmalabs Limited announced the completion of a United States Food and Drug Administration (US FDA) inspection of its Unit-IV facility in Tarapur, Maharashtra, on March 27, 2026.

The inspection concluded with the issuance of a Form 483, which included one observation noted as procedural in nature. Aarti Pharmalabs stated that corrective and preventive actions, along with compliance documentation, will be submitted to the US FDA within the designated timeframe.

The facility inspected was located at Plot No. E-50, 50/1, 59/1, MIDC, Tarapur, Tal. & District Palghar, Maharashtra - 401506. Aarti Pharmalabs’ stock symbol is AARTIPHARM on the National Stock Exchange.

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