FDA Inspection 1063674 — TwinMed, LLC

TwinMed, LLC — FEI 3005086802

The FDA completed an inspection of TwinMed, LLC on Aug 22, 2018 in Santa Fe Springs, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Santa Fe Springs, CA (United States)