FDA Inspection 1144067 — Svelte Medical Systems, Inc.
The FDA completed an inspection of Svelte Medical Systems, Inc. on June 14, 2021 in New Providence, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 14, 2021
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Providence, NJ (United States)