FDA Inspection 998288 — Cardiva Medical Inc.
The FDA completed an inspection of Cardiva Medical Inc. on Dec 15, 2016 in Guaymas. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 15, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Guaymas (Mexico)
Additional details
Postmarket Audit Inspections