FDA Inspection 1078351 — Kelada Creative Group, LLC

Kelada Creative Group, LLC — FEI 3013388272

The FDA completed an inspection of Kelada Creative Group, LLC on Feb 1, 2019 in Houston, 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). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 1, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Houston, TX (United States)

Citations

IDCFRDescription
172221 CFR 211.134(a)Correct labels during finishing operations
176721 CFR 211.137(a)Expiration date lacking
188321 CFR 211.165(a)Testing and release for distribution
359221 CFR 211.110(c)In-process materials characteristics testing

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