FDA Inspection
Lincare, Inc.Lincare, Inc. – FDA Inspection, Jun 11, 2015
Record Details
This FDA Inspection record concerns Lincare, Inc., with an inspection on June 11, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Lincare, Inc.
- Inspection Date
- June 11, 2015
- Product Type
- Drugs
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ID · cde69b42-0334-41e4-a1c7-d62b64e6b75f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 932630
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.198(a)Adverse Drug Experience
- 21 CFR 211.192Quality control unit review of records
- 21 CFR 211.25(a)Training , Education , Experience overall
- 21 CFR 211.150(b)Distribution Recall System
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Other FDA inspections of Lincare, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 19, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Lincare, Inc.
- FDA Inspection 706651 - 2011-01-19
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