FDA inspection
Maxter Glove Manufacturing Sdn Bhd: FDA inspection ending Jun 5, 2003
FDA inspection 282380 · Voluntary Action Indicated (VAI) · Klang, Selangor
Key facts
| Inspection ID | 282380 |
|---|---|
| Firm | Maxter Glove Manufacturing Sdn Bhd |
| FEI number | 3003699698 |
| Address | Lot 6070, Jalan Haji Abdul Manan,, 6th Miles Off Jalan, Meru |
| City | Klang, Selangor |
| Fiscal year | 2003 |
| Inspection end date | Jun 5, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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