FDA Inspection 1103255 — Indivior Manufacturing LLC

Indivior Manufacturing LLC — FEI 3005208599

The FDA completed an inspection of Indivior Manufacturing LLC on Aug 29, 2019 in Raleigh, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 29, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Raleigh, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.