FDA Inspection
Resilience US, Inc.Resilience US, Inc. – FDA Inspection, Sep 25, 2014
Record Details
This FDA Inspection record concerns Resilience US, Inc., with an inspection on September 25, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Resilience US, Inc.
- Inspection Date
- September 25, 2014
- Product Type
- Drugs
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ID · 1b6674da-91e5-456e-afba-1090c029c3cb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 897817
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 314.81(b)(1)(ii)Contamination, chemical or physical change, deterioration
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Other FDA inspections of Resilience US, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 21, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 14, 2017 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 11, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 13, 2009 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 28, 2009 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Resilience US, Inc.
- FDA Inspection 1102300 - 2019-08-21
- FDA Inspection 1028333 - 2017-09-14
- FDA Inspection 1021959 - 2017-08-11
- FDA Inspection 625796 - 2009-11-13
- FDA Inspection 595314 - 2009-05-28
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