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FDA 483 Response for Patheon/Thermo Fisher Inspection – Related EIR and inspection classification letter, FEI: 1018495, Inspection: May 15-24, 2024.
FDA 483 Response for Patheon/Thermo Fisher Inspection – Related EIR and inspection classification letter, FEI: 1018495, Inspection: May 15-24, 2024.
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Original Request: I am requesting a copy of the firm’s 483 response related to the inspection that took place at Patheon/Thermo Fisher in Greenville, NC, as well as the related EIR and inspection classification letter issued thereto. FEI Number: 1018495 Date: May 15-24, 2024 Product Type: Human drugs Please provide the documents electronically if possible.
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- 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. Learn more about Fast-Track Requests here.
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