FDA Inspection 1119401 — Oximeter Plus, Inc
The FDA completed an inspection of Oximeter Plus, Inc on February 20, 2020 in Roslyn Heights, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- February 20, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Roslyn Heights, NY (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3128 | 21 CFR 820.90(a) | Nonconforming product control |
| 486 | 21 CFR 820.50(a) | Evaluation of suppliers, contractors, etc., requirements |