FDA issued a Warning Letter to 86 Harriet Ave Corporation DBA General Devices on 6/1/2016 as a result of this inspection.
483 86 Harriet Ave DBA General Devices Jun 2015
483 86 Harriet Ave DBA General Devices Jun 2015Li Li FDA$119.00 - Available Now
FDA investigators audited the 86 Harriet Ave DBA General Devices - Ridgefield, NJ, United States facility and issued inspectional observations (via FDA 483) on 11 Jun 2015.
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- Category: Medical Devices & Rad Health
- Inspection end: 11 Jun 2015
- Location: Ridgefield, United States
- FEI: 2244646