FDA issued a Warning Letter to ITG-Medev Inc on 9/7/2018 as a result of this inspection.
FDA investigators audited the ITG-Medev - San Francisco, CA, United States facility and issued inspectional observations (via FDA 483) on 06 Jun 2018.
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- Category: Medical Devices & Rad Health
- Inspection end: 06 Jun 2018
- Location: San Francisco, United States
- FEI: 1000307251