FDA Inspection 1265048 — PhytogenX, Inc.

PhytogenX, Inc. — FEI 3006892202

The FDA completed an inspection of PhytogenX, Inc. on Mar 27, 2025 in Morgantown, PA. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 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)

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