FDA issued a Warning Letter to Perma Pure LLC on 9/21/2010 for a previous inspection.
483 Perma Pure Sep 2011

483 Perma Pure Sep 2011

Amy Cramer FDA, Lauren Vajo FDA$119.00 - Available Now

FDA investigators audited the Perma Pure - Lakewood, NJ, United States facility and issued 1 inspectional observation (via FDA 483) on 19 Sep 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 1
  • Inspection end: 19 Sep 2011
  • Location: Lakewood, United States
  • FEI: 2244684
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