FDA inspection
ZEPHYR SLEEP TECHNOLOGIES INC.: FDA inspection ending Dec 8, 2015
FDA inspection 953840 · Voluntary Action Indicated (VAI) · Calgary
Key facts
| Inspection ID | 953840 |
|---|---|
| Firm | ZEPHYR SLEEP TECHNOLOGIES INC. |
| FEI number | 3008960597 |
| Address | 3553 31 St NW Unit 306 |
| City | Calgary |
| Country | Canada |
| Fiscal year | 2016 |
| Inspection end date | Dec 8, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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
- 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