FDA inspection
Lonza Baltimore, Inc.: FDA inspection ending Jul 29, 2005
FDA inspection 388571 · No Action Indicated (NAI) · Baltimore, MD
Key facts
| Inspection ID | 388571 |
|---|---|
| Firm | Lonza Baltimore, Inc. |
| FEI number | 1000512310 |
| Address | 5901 E Lombard St |
| City | Baltimore |
| State | MD |
| ZIP | 21224-6824 |
| Fiscal year | 2005 |
| Inspection end date | Jul 29, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None 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