FDA Inspection
Megafine Pharma (P) LimitedMegafine Pharma (P) Limited – FDA Inspection, Sep 23, 2016
Record Details
This FDA Inspection record concerns Megafine Pharma (P) Limited, with an inspection on September 23, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Megafine Pharma (P) Limited
- Inspection Date
- September 23, 2016
- Product Type
- Drugs
View Company Profile
ID · 44d0f909-d360-496d-a78c-eb1dd8497734
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 988000
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Megafine Pharma (P) Limited
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 21, 2020 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 15, 2018 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 13, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Megafine Pharma (P) Limited
- FDA Inspection 1207908 - 2023-05-12
- FDA Inspection 1121027 - 2020-02-21
- FDA Inspection 1058583 - 2018-06-15
- FDA Inspection 828506 - 2013-03-13
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