# BrightGene Pharmaceutical Co., Ltd., Suzhou, China – FDA Inspections

Source: https://www.keypedia.com/companies/brightgene-pharmaceutical-co-ltd/532f1ca2-79a4-40bb-bf0e-3869fc8a2213

> Inspection records and compliance data for BrightGene Pharmaceutical Co., Ltd. in Suzhou. 4 FDA inspections on record, last inspected April 26, 2024.

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## Details

- Name: BrightGene Pharmaceutical Co., Ltd.
- FEI Number: 3009867839
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Suzhou Industrial Park, Floor C28, C27, C26, C25, No. 218 Xinghu Road; Linhuzhen Wuzhong
- City: Suzhou
- Country Name: China
- Address: Suzhou Industrial Park, Floor C28, C27, C26, C25, No. 218 Xinghu Road; Linhuzhen Wuzhong, Suzhou, China
- Country: China

## Related Documents

- FDA Inspection 1240231 - BrightGene Pharmaceutical Co., Ltd. - 2024-04-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 26, 2024
- [FDA Inspection 1038967 - BrightGene Pharmaceutical Co., Ltd. - 2017-12-08](https://www.keypedia.com/records/fda_inspections/brightgene-pharmaceutical-co-ltd/ee9f58ae-6c34-45c4-8be2-1150961abf5f) — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2017
- FDA Inspection 942083 - BrightGene Pharmaceutical Co., Ltd. - 2015-09-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 10, 2015
- FDA Inspection 831367 - BrightGene Pharmaceutical Co., Ltd. - 2013-03-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2013

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