FDA Inspection
Turbare ManufacturingFDA Inspection 1259059 - Turbare Manufacturing - January 24, 2025
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Record Details
This FDA Inspection record concerns Turbare Manufacturing, with an inspection on January 24, 2025, issued by the Dallas District Office, covering human drugs.
- Office
- Dallas District Office
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ID · 0d7e9368-37a2-4e5c-8858-61dcd15fa8ab
Violation Codes7
21 CFR 211.100(a)21 CFR 211.110(a)21 CFR 211.113(b)21 CFR 211.165(d)21 CFR 211.19221 CFR 211.194(a)(8)21 CFR 211.25(a)
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