FDA Inspection
Midwest Medical ServiceMidwest Medical Service – FDA Inspection, Jan 23, 2014
Record Details
This FDA Inspection record concerns Midwest Medical Service, with an inspection on January 23, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Midwest Medical Service
- Inspection Date
- January 23, 2014
- Product Type
- Drugs
View Company Profile
ID · 328f752e-903d-4871-b813-6781918541d3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 863030
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
8- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.125(f)Procedures Written and Followed
- 21 CFR 211.142Written warehousing procedures established/followed
- 21 CFR 211.125(a)Strict control not exercised over labeling issued
- 21 CFR 211.167(c)Controlled release test methods written, followed
- 21 CFR 211.22(a)Lack of quality control unit
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.150Written distribution procedure
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Midwest Medical Service
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Midwest Medical Service
- FDA Inspection 643340 - 2010-02-03
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