# Shi Heng Technology Co., Ltd. – FDA Inspection, Aug 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/shi-heng-technology-co-ltd/c61d1bdd-5228-4893-8e92-f6fab5916a7d
Source feed: FDA_Inspections

> FDA inspection 987018 of Shi Heng Technology Co., Ltd., August 25, 2016. Classification: Official Action Indicated (OAI). 11 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987018
- Company Name: Shi Heng Technology Co., Ltd.
- Inspection Date: 2016-08-25
- 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: 11

Company: https://www.keypedia.com/companies/shi-heng-technology-co-ltd/8ceacd61-f69a-4f9d-9ca6-693f66f83726

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