FDA inspection
Fei Fah Medical Manufacturing Pte. Ltd.: FDA inspection ending Dec 9, 2015
FDA inspection 955200 · Voluntary Action Indicated (VAI) · Singapore
Key facts
| Inspection ID | 955200 |
|---|---|
| Firm | Fei Fah Medical Manufacturing Pte. Ltd. |
| FEI number | 3003892002 |
| Address | 61 Kaki Bukit Avenue 1, Shun LI Industrial Park |
| City | Singapore |
| Country | Singapore |
| Fiscal year | 2016 |
| Inspection end date | Dec 9, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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