
Aurobindo Pharma Limited has informed the stock exchanges that the United States Food and Drug Administration (USFDA) has completed an inspection at Auroactive Pharma Private Limited, its wholly owned subsidiary.
The inspection concluded with two observations, which the company said will be responded to within the stipulated timeline.
The USFDA conducted the inspection at Auroactive Pharma Private Limited's manufacturing facility in Sancham Village, Ranasthalam Mandal, Srikakulam district, Andhra Pradesh.
The facility manufactures Active Pharmaceutical Ingredients (APIs) and pharmaceutical formulation intermediates. The inspection was carried out from June 22, 2026, to June 26, 2026.
According to the company's filing, the inspection concluded with two observations.
Aurobindo Pharma said it will respond to the observations within the stipulated time.
The company stated that there is no impact on its financials or operations due to the outcome of the inspection.
It also reiterated its commitment to maintaining the highest quality manufacturing standards and said it would keep the stock exchanges informed of any further developments.
Read More: Aurobindo Pharma Share Price in Focus; US FDA Classifies Eugia Unit-III as OAI After Inspection!
As of 25 June 2026, Aurobindo Pharma share price was closed at ₹1,555.20 per share, reflecting a surge of 1.61% from the previous trading session.
Aurobindo Pharma's wholly owned subsidiary, Auroactive Pharma Private Limited, has completed a USFDA inspection that concluded with two observations. The company said it will address the observations within the stipulated timeline and that the inspection has no impact on its financial or operational performance.
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Published on: Jun 27, 2026, 2:57 PM IST

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