FDA Inspection 1208843 — Creodent Prosthetics Ltd.
The FDA completed an inspection of Creodent Prosthetics Ltd. on June 14, 2023 in New York, NY. 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, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New York, NY (United States)