FDA Inspection 976273 — Dhaliwal Labs South LLC

Dhaliwal Labs South LLC — FEI 3007410731

The FDA completed an inspection of Dhaliwal Labs South LLC on Jun 14, 2016 in Dallas, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 14, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dallas, TX (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
202721 CFR 211.192Investigations of discrepancies, failures
434521 CFR 211.160(b)(1)Samples (various types) representative, identified properly

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.