# FDA WARNING_LETTER - Ningbo Smart Pharmaceutical Co. Ltd. - October 29, 2010

Source: https://www.keypedia.com/records/warning_letter/ningbo-smart-pharmaceutical-co-ltd/1fdd59df-a6c1-4bd7-ac8c-367931a1728c

> FDA WARNING_LETTER for Ningbo Smart Pharmaceutical Co. Ltd. on October 29, 2010. Product: Drugs. Access full analysis and detailed observations.

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## Details

- Record Type: WARNING_LETTER
- Company Name: Ningbo Smart Pharmaceutical Co. Ltd.
- Inspection Date: 2010-10-29
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research
- Summary: On March 30, 2011, the FDA issued a Warning Letter to Ningbo Smart Pharmaceutical Co. Ltd. following an October 25-29, 2010 inspection of their API manufacturing facility in Ningbo, China. The inspection revealed significant deviations from Current Good Manufacturing Practice (CGMP), rendering their APIs adulterated under 21 U.S.C. § 351(a)(2)(B).

Key violations included:
1. **Failure of the Quality Control Unit (QCU) to ensure appropriate material testing and reporting:** The QCU approved API batches for release (e.g., (b)(4) USP) without performing required Organic Volatile Impurity (OVI) testing, despite Certificates of Analysis stating conformance. The firm's November 19, 2010 response was deemed insufficient, requiring a comprehensive retrospective review of analytical data and batch records for all products within expiration, and a plan to prevent recurrence, including expanded investigation to all products and comprehensive training.
2. **Failure of the QCU to ensure CGMP compliance and meet specifications:** The QCU released API lots to the U.S. without all required tests, failing to detect inaccurate OVI reporting. Specifically, (b)(4) USP batch #(b)(4) was released without OVI testing, which is required by DMF (b)(4). The firm's explanation of discontinuing OVI

## Related Officers

- [Director](https://www.keypedia.com/people/richard-l-friedman/2827edf4-7dbd-4430-96b2-87853c27e113)

Company: https://www.keypedia.com/companies/ningbo-smart-pharmaceutical-co-ltd/0074b4fd-3de1-4890-ad7c-ed7092036b3d

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
