FDA Inspection 1252413 — PURETEK CORPORATION

PURETEK CORPORATION — FEI 3012818008

The FDA completed an inspection of PURETEK CORPORATION on Oct 24, 2024 in Panorama City, CA. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 24, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Panorama City, CA (United States)

Citations

IDCFRDescription
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
121521 CFR 211.67(b)Written procedures not established/followed

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