FDA inspection
BioReliance Limited: FDA inspection ending Mar 21, 2019
FDA inspection 1091242 · Voluntary Action Indicated (VAI) · Penicuik
Key facts
| Inspection ID | 1091242 |
|---|---|
| Firm | BioReliance Limited |
| FEI number | 3005619544 |
| Address | Pendlands Science Park |
| City | Penicuik |
| Country | United Kingdom |
| Fiscal year | 2019 |
| Inspection end date | Mar 21, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
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