FDA Inspection 1265048 — PhytogenX, Inc.

PhytogenX, Inc. — FEI 3006892202

The FDA completed an inspection of PhytogenX, Inc. on March 27, 2025 in Morgantown, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 27, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morgantown, PA (United States)

Citations

IDCFRDescription
188521 CFR 211.165(b)Microbiological testing
431421 CFR 211.84(d)(2)Reports of Analysis (Components)