FDA WARNING_LETTER - GDMI, Inc - June 29, 2009

FDA WARNING_LETTER for GDMI, Inc on June 29, 2009. Product: Drugs. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for GDMI, Inc on June 29, 2009. Product: Drugs. Access full analysis and detailed observations.

Violation Codes

FD&C Act 501(a)(2)(B)

21 CFR 211.84(d)(2)

21 CFR 211.166(a)

21 CFR 201.128

21 CFR 211.67(b)

21 CFR 211.113(a)

21 CFR 201.66

21 U.S.C. 352(c)

21 U.S.C. 361(c)

21.U.S.C. 355(a)

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Record Information

Company

GDMI, Inc

Inspection Date

June 29, 2009

Product Type

Drugs

Office

Dallas District Office

People

ID: a0f98d3b-d544-4e31-94e7-fecb8ebddf11

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