# FDA Inspection 793138 - Guangzhou Double One Latex Products Co. Ltd - June 21, 2012

Source: https://www.keypedia.com/records/fda_inspections/guangzhou-double-one-latex-products-co-ltd/5777ce9b-0bb4-44ff-880b-ea005a80def2
Source feed: FDA_Inspections

> FDA Inspection 793138 for Guangzhou Double One Latex Products Co. Ltd on June 21, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 793138
- Company Name: Guangzhou Double One Latex Products Co. Ltd
- Inspection Date: 2012-06-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 793138 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/guangzhou-double-one-latex-products-co-ltd/1821bd31-bcdd-47a2-a608-ee19c068c781)

Company: https://www.keypedia.com/companies/guangzhou-double-one-latex-products-co-ltd/401a78d8-8a4f-4406-8b11-af627e3faf66

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7