Zydus Lifesciences has received an Establishment Inspection Report (EIR) from the USFDA for its transdermal manufacturing facility in Ahmedabad, which was inspected in July 2024 and classified as Voluntary Action Indicated (VAI).
AI Assistant
Zydus Lifesciences Ltd
2024
Announcement
Find Answers
Ask about any part of the document to get insights, explanations, or key details.