FDA inspection
PolyPeptide Laboratories (Sweden) AB: FDA inspection ending Apr 10, 2019
FDA inspection 1096761 · Voluntary Action Indicated (VAI) · Limhamn
Key facts
| Inspection ID | 1096761 |
|---|---|
| Firm | PolyPeptide Laboratories (Sweden) AB |
| FEI number | 3002807004 |
| Address | Hogerudsgatan 21 |
| City | Limhamn |
| Country | Sweden |
| Fiscal year | 2019 |
| Inspection end date | Apr 10, 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