FDA Inspection
Sonar Products, Inc.Sonar Products, Inc. – FDA Inspection, Jun 21, 2010
Record Details
This FDA Inspection record concerns Sonar Products, Inc., with an inspection on June 21, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Sonar Products, Inc.
- Inspection Date
- June 21, 2010
- Product Type
- Drugs
View Company Profile
ID · 25934a42-eaaa-40f8-ae3a-92f6ae31f936
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 667709
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
5- 21 CFR 211.198(b)(3)Reason for Not Conducting Complaint Investigation
- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Sonar Products, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 2, 2015 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 12, 2014 | OAI | Center for Drug Evaluation and Research | Unapproved and Misbranded Drugs |
| March 18, 2014 | OAI | Center for Drug Evaluation and Research | Unapproved and Misbranded Drugs |
| February 15, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 9, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sonar Products, Inc.
- FDA Inspection 922999 - 2015-04-02
- FDA Inspection 899650 - 2014-11-12
- FDA Inspection 871333 - 2014-03-18
- FDA Inspection 818381 - 2013-02-15
- FDA Inspection 762450 - 2012-01-09
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