C Chang

Violations of 21 Cfr Part 803 - Medical Device Reporting: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$139.22

Violations of 21 Cfr Part 820 Quality System Regulation: Subpart K- Labeling and Packaging Control, Subpart L- Handling, Storage, Distribution, and Installation, Subpart N- Servicing and Subpart O- St

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$86.51

Violations of 21 Cfr Part 312 - Investigational New Drug Application: Warning Letters Issued by U.S. Food and Drug Administration

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$110.29

Violations Of 21 CFR Part 820 Quality System Regulation, Subparts A-B: General Provisions and Quality System Requirements: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$112.88

Violations Of 21 CFR Part 820 - Quality System Regulation, Subpart J Corrective and Preventive Action: Warning Letters Issued by U.S. Food and Drug Administration

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$138.34

Violations of 21 Cfr Part 820 - Quality System Regulation, Subpart C Design Controls: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$126.67

Violations of 21 Cfr Part 806 - Medical Devices; Reports of Corrections and Removals: Warning Letters Issued by U.S. Food and Drug Administration

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$84.85

Violations of 21 Cfr Part 820 - Quality System Regulation, Subpart M Records: Warning Letters Issued by U.S. Food and Drug Administration

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Out of Stock

Violations of 21 Cfr Part 58 - Good Laboratory Practice for Nonclinical Laboratory: Warning Letters Issued by U.S. Food and Drug Administration

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$84.85

Violations of 21 Cfr Part 56 - Institutional Review Boards: Warning Letters Issued by U.S. Food and Drug Administration

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$85.40

Violations Of 21 CFR Part 820 - Quality System Regulation, Subpart G Production and Process Controls: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$118.99

Violations of 21 Cfr Part 820 Quality System Regulation, Subparts D-F: Document Controls, Purchasing Controls, Identification and Traceability: Warning Letters Issued by U.S. Food and Drug Administrat

C Chang

$101.47

Violations Of 21 CFR Part 820 Quality System Regulation, Subparts H-I: Acceptance Activities and Nonconforming Product: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$126.36

Violations of 21 Cfr Part 812 - Investigational Device Exemptions: Warning Letters Issued by U.S. Food and Drug Administration

C Chang

$136.02