FDA issued a Warning Letter to Frontida BioPharm Inc on 8/15/2016 for a later inspection.
483 Frontida BioPharm Jul 2001

483 Frontida BioPharm Jul 2001

Robert Shibuya FDA$119.00 - Available Now

FDA investigators audited the Frontida BioPharm - Philadelphia, PA, United States facility and issued inspectional observations (via FDA 483) on 27 Jul 2001.

Product details

  • Category: Human Drugs
  • Inspection end: 27 Jul 2001
  • Location: Philadelphia, United States
  • FEI: 2523348
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