483
Veranova LPVeranova LP – FDA 483, Mar 8, 2019
Record Details
The FDA inspection of Johnson Matthey Inc. in West Deptford, NJ, revealed significant deficiencies in equipment maintenance, quality control, and laboratory practices. Issues included a vacuum seal failure leading to product contamination, inadequate investigations into discrepancies, and a failure to follow established test procedures and stability programs. These findings indicate a lack of adherence to cGMP requirements, impacting the quality and purity of drug substances.
View Company Profile
ID · 72912813-3b46-4df7-b84f-283d22efdeae
Other documents for Veranova LP
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.