FDA Inspection 805529 — MyCardio
The FDA completed an inspection of MyCardio on October 22, 2012 in Denver, CO. 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
- October 22, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Denver, CO (United States)