# GUANGDONG BIOLIGHT MEDITECH CO., LTD – FDA Inspection, Mar 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/guangdong-biolight-meditech-co-ltd/a2115671-95fa-4bf5-9d87-4930f5a68e4e
Source feed: FDA_Inspections

> FDA inspection 873587 of GUANGDONG BIOLIGHT MEDITECH CO., LTD, March 20, 2014. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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

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