FDA Inspection
Quintiles IMS Ireland LimitedQuintiles IMS Ireland Limited – FDA Inspection, Sep 15, 2017
Record Details
This FDA Inspection record concerns Quintiles IMS Ireland Limited, with an inspection on September 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d0da964d-62c8-46ed-acc4-c2252e426649
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1025293
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 312.50Ensuring compliance with plan and protocol
- 21 CFR 312.53(d)Selecting monitors
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Other FDA inspections of Quintiles IMS Ireland Limited
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 21, 2010 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Quintiles IMS Ireland Limited
- FDA Inspection 663189 - 2010-05-21
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