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FDA Inspection
•S&B Pharma LLC•March 16, 2018

S&B Pharma LLC – FDA Inspection, Mar 16, 2018

Record Details

This FDA Inspection record concerns S&B Pharma LLC, with an inspection on March 16, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
S&B Pharma LLC
Inspection Date
March 16, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Karen M. Montgomery (Company Rep)
  • Srinivas Chennamaneni (Issuing Officer)
View Company Profile

ID · 9d542333-9374-409a-93d6-381f4b1aa795

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1047928
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

Other FDA inspections of S&B Pharma LLC

9
DateClassificationOfficeProject area
June 17, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 6, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 5, 2019Not classifiedKansas City District OfficeGeneric Drug Evaluation
October 27, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 26, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for S&B Pharma LLC
  • FDA Inspection 1172319 - 2022-06-17
  • FDA Inspection 1121238 - 2020-02-06
  • FDA Inspection 1078320 - 2019-02-05
  • FDA Inspection 1031001 - 2017-10-27
  • FDA Inspection 915801 - 2015-02-26

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