FDA Inspection 1148242 — Captek Softgel Interntional Inc

Captek Softgel Interntional Inc — FEI 3014897154

The FDA completed an inspection of Captek Softgel Interntional Inc on Jun 28, 2021 in La Mirada, 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
Jun 28, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
La Mirada, CA (United States)

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