FDA Inspection 987003 — Argenta US Manufacturing LLC

Argenta US Manufacturing LLC — FEI 1910953

The FDA completed an inspection of Argenta US Manufacturing LLC on Aug 15, 2016 in Shawnee, KS. 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 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shawnee, KS (United States)

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