FDA Inspection 851937 — Heartware, Inc.
The FDA completed an inspection of Heartware, Inc. on August 30, 2013 in Miami Lakes, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 30, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Miami Lakes, FL (United States)