# FDA Inspection 873587 - GUANGDONG BIOLIGHT MEDITECH CO., LTD - March 20, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/guangdong-biolight-meditech-co-ltd/1338677b-81e6-4567-8317-8db1882f92ec
Source feed: FDA_Inspections

> FDA Inspection 873587 for GUANGDONG BIOLIGHT MEDITECH CO., LTD on March 20, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 873587
- Company Name: GUANGDONG BIOLIGHT MEDITECH CO., LTD
- Inspection Date: 2014-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/guangdong-biolight-meditech-co-ltd/a9077544-a39a-4a5f-af41-7b536f0b299f

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