FDA Inspection
Activation Laboratories Ltd.Activation Laboratories Ltd. – FDA Inspection, Sep 10, 2026
Record Details
This FDA Inspection record concerns Activation Laboratories Ltd., with an inspection on September 10, 2026, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · 23f01efc-e759-4ba4-b83c-806419e06b08
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1335136
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.68(b)Computer control of master formula records
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Other FDA inspections of Activation Laboratories Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 14, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 16, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Activation Laboratories Ltd.
- FDA Inspection 1179633 - 2022-08-04
- FDA Inspection 909612 - 2014-11-14
- FDA Inspection 791705 - 2012-07-16
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