# FDA Inspection 999605 - Hebei Pukang Medical Instruments Co., Ltd. - January 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/hebei-pukang-medical-instruments-co-ltd/0b144080-4367-4157-bb1e-1a257f0bb34b
Source feed: FDA_Inspections

> FDA Inspection 999605 for Hebei Pukang Medical Instruments Co., Ltd. on January 12, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999605
- Company Name: Hebei Pukang Medical Instruments Co., Ltd.
- Inspection Date: 2017-01-12
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 999605 - 2017-01-12](https://www.keypedia.com/records/fda_inspections/hebei-pukang-medical-instruments-co-ltd/baa688cc-7c12-4e6f-bf40-fa9b209de292)

Company: https://www.keypedia.com/companies/hebei-pukang-medical-instruments-co-ltd/4c2a5130-0249-4800-8319-02e227be8cad

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