FDA inspection
Keystone Laboratories, Inc.: FDA inspection ending Aug 23, 2005
FDA inspection 393777 · Voluntary Action Indicated (VAI) · Memphis, TN
Key facts
| Inspection ID | 393777 |
|---|---|
| Firm | Keystone Laboratories, Inc. |
| FEI number | 1020139 |
| Address | 1103 Kansas St |
| City | Memphis |
| State | TN |
| ZIP | 38106-1913 |
| Fiscal year | 2005 |
| Inspection end date | Aug 23, 2005 |
| 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
- No Establishment inspection report (EIR) exists
- 10–99 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