CGMP/Active Pharmaceutical Ingredient (API)/Adulterated
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DermaRite Industries Issues Voluntary Nationwide Recall of DermaKleen, Dermasarra, Kleenfoam, and Perigiene Products Due to Burkholderia cepacia Contamination
DermaRite Industries, LLC is voluntarily recalling individual lots of products in the table below due to microbial contamination identified as Burkholderia cepecia.Howard I. Schwartz, M.D. Hollywood, FL. EIR issued 11/19/2020
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 11/19/2020
Short Title (70 char) Howard I. Schwartz, M.D. Hollywood, FL. EIR issued 11/19/2020
FEI Number 1000525885
Firm Name Howard I. Schwartz, M.D.
Record Type EIR
State FL
Establishment Type Clinical InvestF.H. Investments Inc dba Asteria Health. Birmingham, AL. 483 issued 12/19/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 12/19/2025
Short Title (70 char) F.H. Investments Inc dba Asteria Health. Birmingham, AL. 483 issued 12/19/2025
FEI Number 3038253438
Firm Name F.H. Investments Inc dba Asteria Health
Record Type 483
State AL
EsFDA Encourages Development of New, Reliable Alternatives to Animal Testing in Sunscreen
FDA strongly encourages companies to continue to develop new, reliable ways to minimize animal testing and to provide the data necessary for the FDA to make a GRASE determination for sunscreen active ingredients.
