FDA inspection
Sugih Instrumendo Abadi, PT.: FDA inspection ending May 14, 2009
FDA inspection 586556 · No Action Indicated (NAI) · Padalarang, Jawa Barat
Key facts
| Inspection ID | 586556 |
|---|---|
| Firm | Sugih Instrumendo Abadi, PT. |
| FEI number | 3002118752 |
| Address | Jl. Tembokan Rt. 1/01, Ds. Cipeundeuy |
| City | Padalarang, Jawa Barat |
| Country | Indonesia |
| Fiscal year | 2009 |
| Inspection end date | May 14, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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