FDA Inspection 884654 — ReliantHeart Inc.

ReliantHeart Inc. — FEI 3003259341

The FDA completed an inspection of ReliantHeart Inc. on June 30, 2014 in Houston, TX. 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
June 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Houston, TX (United States)