# Hebei Pukang Medical Instruments Co., Ltd. – FDA Inspection, Jan 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/hebei-pukang-medical-instruments-co-ltd/baa688cc-7c12-4e6f-bf40-fa9b209de292
Source feed: FDA_Inspections

> FDA inspection 999605 of Hebei Pukang Medical Instruments Co., Ltd., January 12, 2017. Classification: Official Action Indicated (OAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

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