FDA Inspection
Recipharm HC LimitedRecipharm HC Limited – FDA Inspection, Jan 15, 2016
Record Details
This FDA Inspection record concerns Recipharm HC Limited, with an inspection on January 15, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Recipharm HC Limited
- Inspection Date
- January 15, 2016
- Product Type
- Drugs
View Company Profile
ID · 061059ec-a3a8-458b-b687-d3702d6234b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 956577
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Recipharm HC Limited
6| Date | Classification | Office | Project area |
|---|---|---|---|
| June 27, 2023 | VAI | Office of Inspections and Investigations | |
| November 26, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 10, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 7, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 9, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Recipharm HC Limited
- FDA Inspection 1209510 - 2023-06-27
- FDA Inspection 1156170 - 2020-11-26
- FDA Inspection 1065951 - 2017-11-10
- FDA Inspection 869740 - 2014-03-07
- FDA Inspection 748166 - 2011-09-09
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