FDA Inspection
Arcet Equipment CompanyArcet Equipment Company – FDA Inspection, Jul 21, 2011
Record Details
This FDA Inspection record concerns Arcet Equipment Company, with an inspection on July 21, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Arcet Equipment Company
- Inspection Date
- July 21, 2011
- Product Type
- Drugs
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ID · 0b37791d-4372-433e-b7b9-b7eeab72f3cb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 738148
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Arcet Equipment Company
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 21, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Arcet Equipment Company
- FDA Inspection 782823 - 2012-05-22
- FDA Inspection 737880 - 2011-07-21
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