FDA Inspection 1079308 — PhytogenX, Inc.

PhytogenX, Inc. — FEI 3006892202

The FDA completed an inspection of PhytogenX, Inc. on Feb 14, 2019 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 14, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Morgantown, PA (United States)

Citations

IDCFRDescription
343421 CFR 820.75(c)Documentation - review in response to changes or deviations

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