# FDA Inspection 891775 - Qingdao London Durex Co., Ltd. - July 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/qingdao-london-durex-co-ltd/069a761d-c744-4d33-8a79-29ef2e9a9e56
Source feed: FDA_Inspections

> FDA Inspection 891775 for Qingdao London Durex Co., Ltd. on July 10, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891775
- Company Name: Qingdao London Durex Co., Ltd.
- Inspection Date: 2014-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/qingdao-london-durex-co-ltd/5d427c47-6d2c-426e-a67b-af1df6d416a4

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