FDA Inspection 1122346 — Mercator Medsystems, Inc.
The FDA completed an inspection of Mercator Medsystems, Inc. on January 27, 2020 in San Leandro, CA. 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
- January 27, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- San Leandro, CA (United States)