FDA Form 483 – Human Drug Inspections (4 Firms Listed – June 2024)

FDA Form 483 – Human Drug Inspections (4 Firms Listed – June 2024)

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Original Request: Please provide the FDA-483 documents pertaining to Human DRUG Inspection, for the following 4 firms: Pharmadepot Labs, LLC, 6935 Camino Maquiladora Ste F, San Diego, CA, United States, (FEI: 3017534691), inspection ending 6/18/2024; RK Pharma Inc., 401 N Middletown Rd Bldg 215/215a, Pearl River, NY, United States, (FEI: 3014926340), inspection ending 5/31/2024; Silgan Unicep Packaging Llc, 4122 S Grove Rd, Spokane, WA, United States, (FEI: 3011913386), inspection ending 6/14/2024; Univar Solutions, LLC., 2600 Garfield Ave, Commerce, CA, United States, (FEI: 2015184), inspection ending 4/12/2024.
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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