FDA Inspection
Jubilant Cadista Pharmaceuticals, Inc.Jubilant Cadista Pharmaceuticals, Inc. – FDA Inspection, Mar 23, 2011
Record Details
This FDA Inspection record concerns Jubilant Cadista Pharmaceuticals, Inc., with an inspection on March 23, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- March 23, 2011
- Product Type
- Drugs
View Company Profile
ID · ccf41e68-c202-482c-9eb0-3cd6c9e73349
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 715587
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.165(f)Failing drug products not rejected
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.166(a)Written program not followed
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Other FDA inspections of Jubilant Cadista Pharmaceuticals, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 28, 2020 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| August 7, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 8, 2014 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 1, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 5, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Jubilant Cadista Pharmaceuticals, Inc.
- FDA Inspection 1120136 - 2020-02-28
- FDA Inspection 940733 - 2015-08-07
- FDA Inspection 888209 - 2014-07-08
- FDA Inspection 842669 - 2013-08-01
- FDA Inspection 774268 - 2012-04-05
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