FDA issued a Warning Letter to Peter Schiff Enterprises on 7/31/2013 for a previous inspection.
483 Peter Schiff Enterprises Apr 2017

483 Peter Schiff Enterprises Apr 2017

Mary Millner FDA, Andrew Saunders FDA$119.00 - Available Now

FDA investigators audited the Peter Schiff Enterprises - Cookeville, TN, United States facility and issued inspectional observations (via FDA 483) on 13 Apr 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 13 Apr 2017
  • Location: Cookeville, United States
  • FEI: 1000112898
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