FDA Inspection 998370 — AEGEA MEDICAL INC
The FDA completed an inspection of AEGEA MEDICAL INC on Jan 23, 2017 in Menlo Park, CA. 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
- Jan 23, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Menlo Park, CA (United States)