# Guilin Pharmaceutical Co., Ltd., Guilin, China – FDA Inspections

Source: https://www.keypedia.com/companies/guilin-pharmaceutical-co-ltd/8a53776f-b81a-417d-b1c5-ea1cd2d0b0a8

> Inspection records and compliance data for Guilin Pharmaceutical Co., Ltd. in Guilin. 4 FDA inspections on record, 2 Form 483s, last inspected August 18, 2023.

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## Details

- Name: Guilin Pharmaceutical Co., Ltd.
- FEI Number: 3002807125
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK
- Address Line 1: No. 43 Qilidian Road
- City: Guilin
- Country Name: China
- Address: No. 43 Qilidian Road, Guilin, China
- Country: China

## Related Documents

- [FDA Inspection 1217732 - Guilin Pharmaceutical Co., Ltd. - 2023-08-18](https://www.keypedia.com/records/fda_inspections/guilin-pharmaceutical-co-ltd/330fef8b-c36c-41fe-beb1-3e7344d42db6) — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2023
- [FDA Inspection 1061489 - Guilin Pharmaceutical Co., Ltd. - 2018-07-19](https://www.keypedia.com/records/fda_inspections/guilin-pharmaceutical-co-ltd/b4eb333f-6776-4112-b186-4dad9d53ea0e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 19, 2018
- FDA Inspection 920262 - Guilin Pharmaceutical Co., Ltd. - 2015-03-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 13, 2015
- FDA Inspection 748950 - Guilin Pharmaceutical Co., Ltd. - 2011-09-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 2, 2011

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