FDA Inspection 1149944 — R.D. Laboratories Inc.

R.D. Laboratories Inc. — FEI 1937815

The FDA completed an inspection of R.D. Laboratories Inc. on August 27, 2021 in Washington, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 27, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Washington, MO (United States)

Citations

IDCFRDescription
103321 CFR 211.22(a)Authority lacking to review records, investigate errors
110521 CFR 211.22(d)Procedures not in writing, fully followed
126321 CFR 211.68(b)Computer control of master formula records
356521 CFR 211.58Buildings not maintained in good state of repair