FDA Inspection 1051771 — LODC, Inc.

LODC, Inc. — FEI 3002468914

The FDA completed an inspection of LODC, Inc. on May 2, 2018 in Mercedes, 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). 9 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 2, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Mercedes, TX (United States)

Citations

IDCFRDescription
1544721 CFR 111.15(c)(3)Cleaning compounds and toxic materials - holding
1548021 CFR 111.20(h)Physical plant - screening against pests
1549921 CFR 111.27(a)Equipment - design - suitable
1554321 CFR 111.260(c)Batch record - date, time; maintenance
1574121 CFR 111.210(h)(3)(i)Components, verify weight, measure
1574721 CFR 111.210(g)Packaging description, representative label
1576221 CFR 111.205(a)Master manufacturing record - each batch
1597721 CFR 111.123(a)(1)Quality control operations - master manufacturing record, modifications
1814021 CFR 117.20(b)Plant construction and design

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