FDA issued a Warning Letter to Rapid Release Technologies on 1/17/2017 as a result of this inspection.
483 RAPID RELEASE TECHNOLOGIES May 2016

483 RAPID RELEASE TECHNOLOGIES May 2016

Kirtida Patel FDA$119.00 - Available Now

FDA investigators audited the RAPID RELEASE TECHNOLOGIES - Santa Ana, CA, United States facility and issued 4 inspectional observations (via FDA 483) on 25 May 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 4
  • Inspection end: 25 May 2016
  • Location: Santa Ana, United States
  • FEI: 3009341046
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