FDA issued a Warning Letter to Padtest, LLC on 12/17/2014 as a result of this inspection.
FDA investigators audited the Padtest - Scottsdale, AZ, United States facility and issued 11 inspectional observations (via FDA 483) on 08 Oct 2014.
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- Category: Medical Devices & Rad Health
- Number of Observations: 11
- Inspection end: 08 Oct 2014
- Location: Scottsdale, United States
- FEI: 3007799036