FDA Inspection
Lincare, Inc.Lincare, Inc. – FDA Inspection, Dec 16, 2011
Record Details
This FDA Inspection record concerns Lincare, Inc., with an inspection on December 16, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Lincare, Inc.
- Inspection Date
- December 16, 2011
- Product Type
- Drugs
View Company Profile
ID · 76713fad-9df0-44e5-a2d1-617a962fe312
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 757254
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
5- 21 CFR 211.188(b)(2)Identity of major equipment and lines used
- 21 CFR 211.192Quality control unit review of records
- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of Lincare, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 5, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Lincare, Inc.
- FDA Inspection 784858 - 2012-06-05
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