FDA Inspection
Carilion Materials ManagementCarilion Materials Management – FDA Inspection, Feb 14, 2018
Record Details
This FDA Inspection record concerns Carilion Materials Management, with an inspection on February 14, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 198e384b-1686-462c-b8e1-54ac61136dc6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1041728
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 211.204Record information inclusions
- 21 CFR 211.100(a)Approval and review of procedures
- 21 CFR 211.67(b)Written procedures fail to include
- 21 CFR 211.192No written record of investigation
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Other FDA inspections of Carilion Materials Management
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 16, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 2, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Carilion Materials Management
- FDA Inspection 957601 - 2015-12-16
- FDA Inspection 712034 - 2011-03-02
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