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Following collaboration with FDA, issues related to a cGMP inspection are being resolved
August 17, 2017
By: Kristin Brooks
Managing Editor, Contract Pharma
Valeant Pharmaceuticals received confirmation from the FDA that it intends to issue a Voluntary Action Indicated (VAI) inspection classification for its Bausch + Lomb manufacturing facility in Tampa, FL as part of a forthcoming Establishment Inspection Record for the facility. With this confirmation, manufacturing uncertainties related to current and upcoming regulatory submissions will be eliminated for products manufactured at the Tampa facility. “Following continued close collabor...
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