Cipla's InvaGen US facility gets USFDA inspection closure report
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Cipla's wholly-owned subsidiary InvaGen Pharmaceuticals has received the Establishment Inspection Report (EIR) from the USFDA for its Hauppauge, Long Island, New York manufacturing facility. The EIR indicates closure of the Pre-Approval Inspection conducted earlier in February 2026, suggesting the facility met USFDA requirements without adverse action.
Positive for shareholders: USFDA inspection closure removes regulatory overhang and supports continued US supplies from the facility.