FDA Inspection 1099650 — Greatbatch Medical S. De R.L. De C.V.
The FDA completed an inspection of Greatbatch Medical S. De R.L. De C.V. on August 15, 2019 in Tijuana. 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
- August 15, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tijuana (Mexico)