# FDA 483 - RK Pharma Inc. - March 27, 2026

Source: https://www.keypedia.com/records/483/rk-pharma-inc/9576dafa-346c-44ee-88bc-8c9a293774e1

> FDA 483 for RK Pharma Inc. on March 27, 2026. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: RK Pharma Inc.
- Inspection Date: 2026-03-27
- Product Type: drugs
- Office Name: New York District Office
- Summary: An FDA inspection of Rx Pharma Inc. in Pearl River, NY, revealed significant deficiencies in laboratory controls and investigation procedures for drug product manufacturing. The firm failed to ensure the reliability of its visual inspection process for detecting particulates and critical defects, and its investigations into recurring non-viable particle count excursions and out-of-specification results were inadequate. These issues indicate a potential compromise in drug product quality and purity due to a lack of proper root cause analysis and effective corrective actions.

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## Related Officers

- [Lata C. Mathew](https://www.keypedia.com/people/lata-c-mathew/0610a0ef-dcc5-43e7-ab74-2ac54d758beb)
- [Robin P. Mathew](https://www.keypedia.com/people/robin-p-mathew/35f4a085-58b8-4208-a648-ef2d533e1ece)
- [Robin P. Mathew, Investigator](https://www.keypedia.com/people/robin-p-mathew-investigator/1d49a8f2-6832-48c3-b067-eac4788625c4)

Company: https://www.keypedia.com/companies/rk-pharma-inc/04d6c855-6dac-45ed-8597-0541bddd3bce

Office: https://www.keypedia.com/offices/new-york-district-office/9fa3d265-16ca-438d-8a6e-b47f60dc260d
