FDA issued a Warning Letter to One Way Drug, LLC on 7/22/2015 as a result of this inspection.
FDA investigators audited the One Way Drug - Las Vegas, NV, United States facility and issued 7 inspectional observations (via FDA 483) on 30 May 2014.
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- Category: Human Drugs
- Number of Observations: 7
- Inspection end: 30 May 2014
- Location: Las Vegas, United States
- FEI: 3010839113