FDA inspection
Katayama Seiyakusyo Co., Ltd., Toyama Plant: FDA inspection ending Oct 21, 2004
FDA inspection 358195 · Voluntary Action Indicated (VAI) · Toyama
Key facts
| Inspection ID | 358195 |
|---|---|
| Firm | Katayama Seiyakusyo Co., Ltd., Toyama Plant |
| FEI number | 3004349300 |
| Address | 1 Chome 3, Yatsuomachiyasuuchi |
| City | Toyama |
| Fiscal year | 2005 |
| Inspection end date | Oct 21, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
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