# Huatai Biopharm Inc., Deyang, China – FDA Inspections

Source: https://www.keypedia.com/companies/huatai-biopharm-inc/472dd7e5-00b0-4424-bf15-12f621f7cc3f

> Inspection records and compliance data for Huatai Biopharm Inc. in Deyang. 5 FDA inspections on record, 1 Form 483, last inspected September 19, 2025.

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## Details

- Name: Huatai Biopharm Inc.
- FEI Number: 3007783546
- Business Operations: API MANUFACTURE
- Address Line 1: Industrial Park, Xiaohan Town
- City: Deyang
- Country Name: China
- Address: Industrial Park, Xiaohan Town, Deyang, China
- Country: China

## Related Documents

- [FDA Inspection 1288714 - Huatai Biopharm Inc. - 2025-09-19](https://www.keypedia.com/records/fda_inspections/huatai-biopharm-inc/4563f6c5-ee00-420e-b42f-5b2b4cc3bd67) — source: FDA, date: September 19, 2025
- FDA Inspection 1288714 - Huatai Biopharm Inc. - 2025-09-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 19, 2025
- FDA Inspection 1144990 - Huatai Biopharm Inc. - 2019-05-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2019
- FDA Inspection 979665 - Huatai Biopharm Inc. - 2016-06-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 17, 2016
- FDA Inspection 879315 - Huatai Biopharm Inc. - 2014-04-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2014
- FDA Inspection 617852 - Huatai Biopharm Inc. - 2009-09-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 10, 2009

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