FDA Inspection 782342 — Advent Medical Products, Inc.
The FDA completed an inspection of Advent Medical Products, Inc. on May 17, 2012 in Cambridge, MA. 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
- May 17, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cambridge, MA (United States)