FDA Inspection 1203079 — P2Life

P2Life — FEI 3012786818

The FDA completed an inspection of P2Life on Apr 21, 2023 in Cape Town. 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: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 21, 2023
Fiscal Year
2023
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Cape Town (South Africa)

Citations

IDCFRDescription
1576121 CFR 111.205(b)(1)Master manufacturing record - specifications; quality
1580921 CFR 111.570(b)(1)Written procedures - product complaint; review, investigate
1583921 CFR 111.70(e)Specifications - identity, purity, strength, composition
1592721 CFR 111.103Written procedures - quality control operations

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