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FDA Inspection
•A-S Medication Solutions LLC•October 22, 2009

A-S Medication Solutions LLC – FDA Inspection, Oct 22, 2009

Record Details

This FDA Inspection record concerns A-S Medication Solutions LLC, with an inspection on October 22, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
A-S Medication Solutions LLC
Inspection Date
October 22, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 61375744-f97d-4fe9-aeb3-03d5f2794264

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
628529
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

8
  1. 21 CFR 211.100(a)Changes to Procedures Not Reviewed, Approved
  2. 21 CFR 211.192Quality control unit review of records
  3. 21 CFR 211.198(a)Complaint Handling Procedure
  4. 21 CFR 211.170(b)Annual visual exams of drug products
  5. 21 CFR 211.160(b)(4)Calibration - at intervals, written program, remedial action
  6. 21 CFR 211.130(c)Lot or control number assigned
  7. 21 CFR 211.170(b)Reserve drug product sample quantity - all tests
  8. 21 CFR 211.142(a)Quarantine - written procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of A-S Medication Solutions LLC

8
DateClassificationOfficeProject area
August 12, 2026Not classifiedChicago District OfficeDrug Quality Assurance
February 16, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 8, 2022NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
June 5, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 23, 2017NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
View all 8 other inspections on the company page
Other documents for A-S Medication Solutions LLC
  • FDA Inspection 1331612 - 2026-08-12
  • FDA Inspection 1199213 - 2023-02-16
  • FDA Inspection 1172338 - 2022-06-08
  • FDA Inspection 1054512 - 2018-06-05
  • FDA Inspection 1031726 - 2017-10-23

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