FDA Inspection
GUANGDONG BIOLIGHT MEDITECH CO., LTDGUANGDONG BIOLIGHT MEDITECH CO., LTD – FDA Inspection, Oct 12, 2017
Record Details
This FDA Inspection record concerns GUANGDONG BIOLIGHT MEDITECH CO., LTD, with an inspection on October 12, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- October 12, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 76f9e03d-329a-43c6-9103-127adb52ff2c
Inspection Facts
- Inspection number
- 1043345
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of GUANGDONG BIOLIGHT MEDITECH CO., LTD
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 5, 2024 | Not classified | Office of Inspections and Investigations | Compliance: Medical Devices |
| April 14, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 20, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for GUANGDONG BIOLIGHT MEDITECH CO., LTD
- FDA Inspection 1249761 - 2024-09-05
- FDA Inspection 977307 - 2016-04-14
- FDA Inspection 873587 - 2014-03-20
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