FDA issued a Warning Letter to Peter Schiff Enterprises on 7/31/2013 as a result of this inspection.
FDA investigators audited the Peter Schiff Enterprises - Cookeville, TN, United States facility and issued 5 inspectional observations (via FDA 483) on 12 Apr 2013.
Product details
- Category: Medical Devices & Rad Health
- Number of Observations: 5
- Inspection end: 12 Apr 2013
- Location: Cookeville, United States
- FEI: 1000112898
