FDA Inspection 1057670 — PureOxyWash, Inc.

PureOxyWash, Inc. — FEI 3013680093

The FDA completed an inspection of PureOxyWash, Inc. on June 22, 2018 in Burke, VA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Burke, VA (United States)