FDA Inspection 1037949 — Rinovum Subsidiary 2 LLC

Rinovum Subsidiary 2 LLC — FEI 3015417614

The FDA completed an inspection of Rinovum Subsidiary 2 LLC on November 17, 2017 in Monroeville, PA. 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
November 17, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Monroeville, PA (United States)

Additional Details

Sponsor, Contract Research Organization