FDA Inspection 1112500 — DyAnsys India Pvt. Ltd.
The FDA completed an inspection of DyAnsys India Pvt. Ltd. on November 14, 2019 in Chennai. 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
- November 14, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chennai (India)