FDA inspection
Evonik Corporation: FDA inspection ending Aug 10, 2018
FDA inspection 1063207 · Voluntary Action Indicated (VAI) · Birmingham, AL
Key facts
| Inspection ID | 1063207 |
|---|---|
| Firm | Evonik Corporation |
| FEI number | 3012757951 |
| Address | 750 Lakeshore Pkwy |
| City | Birmingham |
| State | AL |
| ZIP | 35211 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Aug 10, 2018 |
| 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
- Yes 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