# FujiFilm Ultra Pure Solutions, Inc. – FDA Inspection, Jan 12, 2017

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

> FDA inspection 996404 of FujiFilm Ultra Pure Solutions, Inc., January 12, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 211. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 4

## Related Documents

- FDA Inspection 1116146 - 2020-01-15
- FDA Inspection 678306 - 2010-09-01

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/massoud-motamed/a8b363de-eb95-4bd3-8c05-9c34bbdbdc8a)

Company: https://www.keypedia.com/companies/fujifilm-ultra-pure-solutions-inc/958bdfeb-69bc-412d-b79e-2cfcb8615ef6

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