FDA Inspection
Sumitomo Pharma America, Inc.Sumitomo Pharma America, Inc. – FDA Inspection, Sep 1, 2009
Record Details
This FDA Inspection record concerns Sumitomo Pharma America, Inc., with an inspection on September 1, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 1, 2009
- Product Type
- Drugs
View Company Profile
ID · bf1aa7f0-a205-4cab-af6d-6d2c250315a8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 608872
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
Other FDA inspections of Sumitomo Pharma America, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| August 2, 2024 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| November 5, 2021 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| January 23, 2015 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| May 24, 2013 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| December 9, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sumitomo Pharma America, Inc.
- FDA Inspection 1242239 - 2024-08-02
- FDA Inspection 1161579 - 2021-11-05
- FDA Inspection 915063 - 2015-01-23
- FDA Inspection 843011 - 2013-05-24
- FDA Inspection 759431 - 2011-12-09
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