FDA Inspection 971061 — Argon Medical Devices Inc.
The FDA completed an inspection of Argon Medical Devices Inc. on May 4, 2016 in Wheeling, IL. 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 4, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Wheeling, IL (United States)