FDA inspection
CK Products, LLC: FDA inspection ending May 20, 2004
FDA inspection 363367 · Fort Wayne, IN
Key facts
| Inspection ID | 363367 |
|---|---|
| Firm | CK Products, LLC |
| FEI number | 1831092 |
| Address | 6230 Innovation Blvd |
| City | Fort Wayne |
| State | IN |
| ZIP | 46818-1399 |
| Fiscal year | 2004 |
| Inspection end date | May 20, 2004 |
| Product type | Food/Cosmetics |
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