FDA Inspection
Intermax Pharmaceuticals, Inc.Intermax Pharmaceuticals, Inc. – FDA Inspection, Nov 28, 2011
Record Details
This FDA Inspection record concerns Intermax Pharmaceuticals, Inc., with an inspection on November 28, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 28, 2011
- Product Type
- Drugs
View Company Profile
ID · 13ec96e5-3c35-4bc2-81df-0f8fae43900d
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 754912
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Intermax Pharmaceuticals, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2012 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 8, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 28, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 3, 2009 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Intermax Pharmaceuticals, Inc.
- FDA Inspection 768948 - 2012-02-21
- FDA Inspection 696893 - 2010-11-08
- FDA Inspection 659964 - 2010-04-28
- FDA Inspection 560581 - 2009-02-03
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