FDA Inspection
State of New Mexico Department of Health, Pharmacy DivisionState of New Mexico Department of Health, Pharmacy Division – FDA Inspection, Jan 16, 2009
Record Details
This FDA Inspection record concerns State of New Mexico Department of Health, Pharmacy Division, with an inspection on January 16, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- January 16, 2009
- Product Type
- Drugs
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ID · 501e2c12-590f-4830-bbec-5451cd48d291
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 557223
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
5- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.192Written record of investigation incomplete
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