FDA Inspection 1018125 — Mohammed Siddique Tayob

Mohammed Siddique Tayob — FEI 3013395067

The FDA completed an inspection of Mohammed Siddique Tayob on Jun 30, 2017 in Middleburg 1050. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 30, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Middleburg 1050 (South Africa)

Additional details

Clinical Investigator (CI)

Citations

IDCFRDescription
752621 CFR 312.62(a)Accountability records
756021 CFR 312.60FD-1572, protocol compliance

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