FDA Inspection
I. L. Bevill Company, Inc.I. L. Bevill Company, Inc. – FDA Inspection, Feb 25, 2013
Record Details
This FDA Inspection record concerns I. L. Bevill Company, Inc., with an inspection on February 25, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- I. L. Bevill Company, Inc.
- Inspection Date
- February 25, 2013
- Product Type
- Drugs
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ID · bd2beb76-b0c3-4574-b82f-2525c576903a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819750
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
15- 21 CFR 211.150(b)Recall facilitation
- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.137(a)Expiration date lacking
- 21 CFR 211.84(a)Components withheld from use pending release
- 21 CFR 211.65(a)Equipment construction - reactive surfaces
- 21 CFR 211.170(b)Investigation of reserve sample deterioration
- 21 CFR 211.130(d)Examination of packaging and labeling
- 21 CFR 211.198(a)Procedures to be written and followed
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
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