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GUANGDONG BIOLIGHT MEDITECH CO., LTD Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

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GUANGDONG BIOLIGHT MEDITECH CO., LTD

Zhuhai, -, China
Issue DateMarch 20, 2014
FEI Number3007305624
CountryChina
Status
No Warning Letter
Product Type
Devices
GUANGDONG BIOLIGHT MEDITECH CO., LTD FDA Form 483, Zhuhai, March 20, 2014