FDA Inspection
Midway Medical Products, Inc.Midway Medical Products, Inc. – FDA Inspection, Jun 16, 2011
Record Details
This FDA Inspection record concerns Midway Medical Products, Inc., with an inspection on June 16, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- June 16, 2011
- Product Type
- Biologics
View Company Profile
ID · e535fc35-618d-4311-a401-2f7cd1dfe086
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 731378
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.265(c)(1)Release of HCT/Ps by responsible person
- 21 CFR 1271.320(a)Procedures re complaints
- 21 CFR 1271.260(e)Storage temperatures recorded, maintained
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Other FDA inspections of Midway Medical Products, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 22, 2013 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 22, 2009 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Midway Medical Products, Inc.
- FDA Inspection 856462 - 2013-11-22
- FDA Inspection 590932 - 2009-06-22
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