FDA inspection
GUANGDONG BIOLIGHT MEDITECH CO., LTD: FDA inspection ending Apr 14, 2016
FDA inspection 977307 · No Action Indicated (NAI) · Zhuhai
Key facts
| Inspection ID | 977307 |
|---|---|
| Firm | GUANGDONG BIOLIGHT MEDITECH CO., LTD |
| FEI number | 3007305624 |
| Address | Technology Innovation Coast Hi, No. 2 Innovation First Road; Tech Zone |
| City | Zhuhai |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Apr 14, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data