FDA Inspection 1079834 — Sixarp, LLC

Sixarp, LLC — FEI 1000115322

The FDA completed an inspection of Sixarp, LLC on Feb 5, 2019 in Grand Rapids, MI. 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
Feb 5, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Rapids, MI (United States)

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