FDA Inspection 1028333 — Resilience US, Inc.

Resilience US, Inc. — FEI 1000305672

The FDA completed an inspection of Resilience US, Inc. on September 14, 2017 in Allston, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Allston, MA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)