FDA Inspection
NorMedNorMed – FDA Inspection, Dec 12, 2012
Record Details
This FDA Inspection record concerns NorMed, with an inspection on December 12, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- NorMed
- Inspection Date
- December 12, 2012
- Product Type
- Drugs
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ID · d80fec33-940b-437f-af26-22afe0b4ba8e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 809893
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.130Procedures are written, and followed
- 21 CFR 211.122(a)Written procedures describing in detail
- 21 CFR 211.150Written distribution procedure
Full citation text and observation details available on the Dashboard.
Other FDA inspections of NorMed
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 29, 2025 | VAI | Seattle District Office | Drug Quality Assurance |
| January 16, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 22, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for NorMed
- FDA Inspection 1271198 - 2025-05-29
- FDA Inspection 1037662 - 2018-01-16
- FDA Inspection 734357 - 2011-06-22
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