FDA Inspection
Arcet Equipment Company, Inc.Arcet Equipment Company, Inc. – FDA Inspection, Jun 8, 2010
Record Details
This FDA Inspection record concerns Arcet Equipment Company, Inc., with an inspection on June 8, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- June 8, 2010
- Product Type
- Drugs
View Company Profile
ID · 474b8c54-b3a9-4a22-83fe-417d7f82153c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 667712
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.165(a)Testing and release for distribution
- 21 CFR 211.100(a)Absence of Written Procedures
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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