FDA Inspection
GUANGDONG BIOLIGHT MEDITECH CO., LTDGUANGDONG BIOLIGHT MEDITECH CO., LTD – FDA Inspection, Sep 5, 2024
Record Details
This FDA Inspection record concerns GUANGDONG BIOLIGHT MEDITECH CO., LTD, with an inspection on September 5, 2024, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 5, 2024
- Product Type
- Medical Devices & Rad Health
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ID · e5776036-1bf6-46d0-95a6-90d2fea8cd95
Inspection Facts
- Inspection number
- 1249761
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
FDA Citations
2- 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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Other FDA inspections of GUANGDONG BIOLIGHT MEDITECH CO., LTD
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 12, 2017 | Not classified | Office of Inspections and Investigations | |
| 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 1043345 - 2017-10-12
- FDA Inspection 977307 - 2016-04-14
- FDA Inspection 873587 - 2014-03-20
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