FDA Inspection 1102533 — Isorx Corp

Isorx Corp — FEI 3006624492

The FDA completed an inspection of Isorx Corp on September 18, 2019 in Richmond, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 18, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Richmond, CA (United States)