FDA Inspection
Radpharm, Inc.Radpharm, Inc. – FDA Inspection, Aug 31, 2010
Record Details
This FDA Inspection record concerns Radpharm, Inc., with an inspection on August 31, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Radpharm, Inc.
- Inspection Date
- August 31, 2010
- Product Type
- Drugs
View Company Profile
ID · 26d95ae9-5e62-439c-80ec-1fcfc10b1c68
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 681204
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
5- 21 CFR 312.53(c)(4)Financial information - commitment to update
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
- 21 CFR 312.50General responsibilities of sponsors
- 21 CFR 312.53(a)Investigator selection
- 21 CFR 312.57(c)Record retention requirement
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Other FDA inspections of Radpharm, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 17, 2011 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| May 11, 2011 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Radpharm, Inc.
- FDA Inspection 756928 - 2011-11-17
- FDA Inspection 724924 - 2011-05-11
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