FDA inspection
Douglas Manufacturing Limited: FDA inspection ending Oct 11, 2019
FDA inspection 1110387 · Voluntary Action Indicated (VAI) · Auckland
Key facts
| Inspection ID | 1110387 |
|---|---|
| Firm | Douglas Manufacturing Limited |
| FEI number | 3005641565 |
| Address | Cnr Te Pai Place & Central Park Drive, Lincoln |
| City | Auckland |
| Country | New Zealand |
| Fiscal year | 2020 |
| Inspection end date | Oct 11, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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