# FDA Inspection 996404 - FujiFilm Ultra Pure Solutions, Inc. - January 12, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-ultra-pure-solutions-inc/7882f518-e6a7-4848-afea-06a662f35a0a
Source feed: FDA_Inspections

> FDA Inspection 996404 for FujiFilm Ultra Pure Solutions, Inc. on January 12, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996404
- Company Name: FujiFilm Ultra Pure Solutions, Inc.
- Inspection Date: 2017-01-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c