FDA Inspection
The Sun Products CorporationThe Sun Products Corporation – FDA Inspection, Nov 19, 2009
Record Details
This FDA Inspection record concerns The Sun Products Corporation, with an inspection on November 19, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- The Sun Products Corporation
- Inspection Date
- November 19, 2009
- Product Type
- Drugs
View Company Profile
ID · 3a6f70a9-4fff-491f-b342-1d4a27d82db8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 629931
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.188(b)(8)Labeling control records including specimens or copies
- 21 CFR 211.137(a)Expiration date lacking
- 21 CFR 211.194(a)Complete test data included in records
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
Full citation text and observation details available on the Dashboard.
Other FDA inspections of The Sun Products Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 9, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 9, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for The Sun Products Corporation
- FDA Inspection 981567 - 2016-08-09
- FDA Inspection 766944 - 2012-02-09
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.