# FDA 483 - Veranova LP - March 08, 2019

Source: https://www.globalkeysolutions.net/records/483/veranova-lp/72912813-3b46-4df7-b84f-283d22efdeae

> FDA 483 for Veranova LP on March 08, 2019. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Veranova LP
- Inspection Date: 2019-03-08
- Product Type: drugs
- Office Name: New Jersey District Office
- Summary: 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.

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## Related Officers

- [Investigator](https://www.globalkeysolutions.net/people/nancy-m-espinal/f4494790-6a37-4998-853c-f859a0eb3330)

Company: https://www.globalkeysolutions.net/companies/veranova-lp/22f7ea09-da55-4ee1-aa40-fce66fa3ef61

Office: https://www.globalkeysolutions.net/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248