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Symbiotec Pharmalab receives EIR from USFDA for Pithampur facility with VAI status

29 Sep 2026 Evaluate

Symbiotec Pharmalab has received the establishment inspection report (EIR) from the U.S. Food and Drug Administration (USFDA) for its manufacturing facility in Pithampur (SEZ), Madhya Pradesh India with a Voluntary Action Indicated (VAI) status. The inspection was conducted at the company’s manufacturing facility at Pithampur, from August 10, 2026 to August 14, 2026.

Symbiotec Pharmalab is a research and development-driven, science-based pharmaceutical and biotechnology company with capabilities across three platforms - organic chemistry, biotechnology and complex injectables.

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