# Guangzhou Able Entertainment Lighting Equipment Co., Ltd., Guangzhou, China – FDA Inspections

Source: https://www.keypedia.com/companies/guangzhou-able-entertainment-lighting-equipment-co-ltd/4a021e41-75ff-45ab-859b-22d9bb4ceedf

> Inspection records and compliance data for Guangzhou Able Entertainment Lighting Equipment Co., Ltd. in Guangzhou. 5 FDA inspections on record (1 OAI), last inspected May 30, 2025.

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## Details

- Name: Guangzhou Able Entertainment Lighting Equipment Co., Ltd.
- FEI Number: 3007610731
- Address Line 1: SHIJING TOWN, BIAYUN DISTRICT, 3 FLOOR, C HOUSE, HUAMING INDUSTRIAL PARK, HUANJIAO VILLAGE
- City: Guangzhou
- Country Name: China
- Address: SHIJING TOWN, BIAYUN DISTRICT, 3 FLOOR, C HOUSE, HUAMING INDUSTRIAL PARK, HUANJIAO VILLAGE, Guangzhou, China
- Country: China

## Related Documents

- FDA Inspection 1284684 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2025-05-30 — source: FDA, date: May 30, 2025
- FDA Inspection 1284684 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2025-05-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 30, 2025
- FDA Inspection 1099880 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2019-05-24 — source: FDA, date: May 24, 2019
- [FDA Inspection 956435 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2015-12-07](https://www.keypedia.com/records/fda_inspections/guangzhou-able-entertainment-lighting-equipment-co-ltd/4d608fe0-df60-4c81-94f5-28c41c291985) — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2015
- FDA Inspection 886836 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2014-04-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2014
- [FDA Inspection 764096 - Guangzhou Able Entertainment Lighting Equipment Co., Ltd. - 2011-11-30](https://www.keypedia.com/records/fda_inspections/guangzhou-able-entertainment-lighting-equipment-co-ltd/b691001f-7344-4346-925f-9564a66688b0) — classification: Official Action Indicated (OAI), source: FDA, date: November 30, 2011

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