FDA Inspection
ILS LimitedILS Limited – FDA Inspection, Mar 7, 2017
Record Details
This FDA Inspection record concerns ILS Limited, with an inspection on March 7, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · c7026aeb-6ffd-4a21-8e6d-772c914ed8f5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1005166
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 211.194(a)(4)Complete Test Data
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.192No written record of investigation
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Other FDA inspections of ILS Limited
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 23, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 9, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for ILS Limited
- FDA Inspection 879676 - 2014-05-23
- FDA Inspection 698139 - 2010-11-09
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