FDA Inspection
MasterPharm LLCMasterPharm LLC – FDA Inspection, Jan 30, 2017
Record Details
This FDA Inspection record concerns MasterPharm LLC, with an inspection on January 30, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ed46c4aa-20ad-4b33-901e-c3e687aa3527
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1000203
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
- Enforcement
- State Referral Letter
Other FDA inspections of MasterPharm LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2020 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 6, 2015 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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