FDA Inspection
Leio CorporationLeio Corporation – FDA Inspection, May 1, 2013
Record Details
This FDA Inspection record concerns Leio Corporation, with an inspection on May 1, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Leio Corporation
- Inspection Date
- May 1, 2013
- Product Type
- Drugs
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ID · 7e8b05dc-cfc3-437d-8bd5-06272fe47253
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 830606
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.150(b)Distribution Recall System
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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