FDA Inspection 1263548 — Asclemed USA Inc.

Asclemed USA Inc. — FEI 3001452204

The FDA completed an inspection of Asclemed USA Inc. on Mar 5, 2025 in Torrance, CA. 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
Mar 5, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Torrance, CA (United States)

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