FDA Inspection
Lorch UlrikeLorch Ulrike – FDA Inspection, Jun 21, 2013
Record Details
This FDA Inspection record concerns Lorch Ulrike, with an inspection on June 21, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Lorch Ulrike
- Inspection Date
- June 21, 2013
- Product Type
- Drugs
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ID · b80c23c0-7503-4c5c-b860-b10bfc13ee38
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 840227
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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