# FDA Inspection 948403 - Wonjin Mulsan Co., Ltd. - October 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/wonjin-mulsan-co-ltd/3b67ac61-a928-4276-a759-493be6d37e43
Source feed: FDA_Inspections

> FDA Inspection 948403 for Wonjin Mulsan Co., Ltd. on October 22, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 948403
- Company Name: Wonjin Mulsan Co., Ltd.
- Inspection Date: 2015-10-22
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 828626 - 2013-04-04](https://www.keypedia.com/records/fda_inspections/wonjin-mulsan-co-ltd/0e3f035b-9a1e-4f44-8913-2e3ebfc1effb)
- [FDA Inspection 828626 - 2013-04-04](https://www.keypedia.com/records/fda_inspections/wonjin-mulsan-co-ltd/be32fc73-6f64-482d-bbc7-630a4c51c257)

Company: https://www.keypedia.com/companies/wonjin-mulsan-co-ltd/6b48e2e6-05e3-430b-9a7e-e4b3c7e1d79b

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