FDA Inspection
Neumann's Home Medical Equipment, Inc.Neumann's Home Medical Equipment, Inc. – FDA Inspection, Jul 29, 2011
Record Details
This FDA Inspection record concerns Neumann's Home Medical Equipment, Inc., with an inspection on July 29, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 29, 2011
- Product Type
- Drugs
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ID · aa24c0c0-abbe-43c8-a9cb-493e37190831
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 738282
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.165(a)Testing and release for distribution
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Neumann's Home Medical Equipment, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 26, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Neumann's Home Medical Equipment, Inc.
- FDA Inspection 894615 - 2014-08-26
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