FDA Inspection 932050 — Henry Schein Inc.
The FDA completed an inspection of Henry Schein Inc. on Jun 23, 2015 in Melville, NY. 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
- Jun 23, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Melville, NY (United States)