FDA Inspection
Kindeva Drug Delivery LPKindeva Drug Delivery LP – FDA Inspection, Feb 12, 2010
Record Details
This FDA Inspection record concerns Kindeva Drug Delivery LP, with an inspection on February 12, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Kindeva Drug Delivery LP
- Inspection Date
- February 12, 2010
- Product Type
- Drugs
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ID · 9807fa4e-d44d-4ac1-a932-b78ea3cf7ead
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 645889
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.67(b)Written procedures fail to include
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Kindeva Drug Delivery LP
11| Date | Classification | Office | Project area |
|---|---|---|---|
| November 13, 2025 | VAI | Los Angeles District Office | Drug Quality Assurance |
| July 28, 2021 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 25, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 25, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 6, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Kindeva Drug Delivery LP
- FDA Inspection 1286864 - 2025-11-13
- FDA Inspection 1151074 - 2021-07-28
- FDA Inspection 1082205 - 2019-01-25
- FDA Inspection 1077108 - 2019-01-25
- FDA Inspection 1008836 - 2017-03-06
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