FDA inspection
Lockheed-Martin Aculight: FDA inspection ending May 21, 2009
FDA inspection 584821 · Bothell, WA
Key facts
| Inspection ID | 584821 |
|---|---|
| Firm | Lockheed-Martin Aculight |
| FEI number | 3003346474 |
| Address | 22121 20th Ave SE |
| City | Bothell |
| State | WA |
| ZIP | 98021-4408 |
| Fiscal year | 2009 |
| Inspection end date | May 21, 2009 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
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