FDA Inspection 1302474 — Redrose Manufacturing Ltd

Redrose Manufacturing Ltd — FEI 3005280521

The FDA completed an inspection of Redrose Manufacturing Ltd on Jan 29, 2026 in Houghton Le Spring. 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
Jan 29, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Houghton Le Spring (United Kingdom)

Citations

IDCFRDescription
1586121 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
1598421 CFR 111.123(a)(8)Quality control - finished batch, distribution
2282321 CFR 111.15(b)Physical plant - clean and sanitary
2283721 CFR 111.27(d)Equipment - maintain - general

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