FDA inspection
Mckesson Drug Company: FDA inspection ending Jul 28, 2017
FDA inspection 1029919 · Voluntary Action Indicated (VAI) · Duluth, GA
Key facts
| Inspection ID | 1029919 |
|---|---|
| Firm | Mckesson Drug Company |
| FEI number | 1030548 |
| Address | 2975 Evergreen Dr |
| City | Duluth |
| State | GA |
| ZIP | 30096 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jul 28, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
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