FDA issued a Warning Letter to Peter Schiff Enterprises on 7/31/2013 for a later inspection.
483 Peter Schiff Enterprises Dec 2011

483 Peter Schiff Enterprises Dec 2011

$119 - Not in Stock

FDA investigators audited the Peter Schiff Enterprises - Cookeville, TN, United States facility and issued inspectional observations (via FDA 483) on 07 Dec 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 07 Dec 2011
  • Location: Cookeville, United States
  • FEI: 1000112898
Order