FDA issued a Warning Letter to Diasol Inc on 9/28/2017 as a result of this inspection.
FDA investigators audited the Diasol - Phillipsburg, NJ, United States facility and issued inspectional observations (via FDA 483) on 15 Jun 2017.
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- Category: Medical Devices & Rad Health
- Inspection end: 15 Jun 2017
- Location: Phillipsburg, United States
- FEI: 3009491770