FDA Form 483s for Mannkind, Hologic, Sterigenics, and Others – Devices Inspections

FDA Form 483s for Mannkind, Hologic, Sterigenics, and Others – Devices Inspections

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Original Request: Please provide the following inspection-related document(s) in electronic PDF format for product type Devices: The 483(s) (in electronic format) for the inspection of Mannkind Corporation (FEI 3003154078), located in Marlborough, Massachusetts, United States, inspection ending 2024-10-03. The 483(s) (in electronic format) for the inspection of Hologic, Inc (FEI 1000120743), located in Marlborough, Massachusetts, United States, inspection ending 2024-09-24. The 483(s) (in electronic format) for the inspection of Sterigenics Radiation Technologies IN, Inc (FEI 3009504230), located in Columbia City, Indiana, United States, inspection ending 2024-09-19. etc
Tags: MedTech, 483, 2024
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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