FDA Inspection 1327240 — Sentry Manufacturing, Inc.

Sentry Manufacturing, Inc. — FEI 1051353

The FDA completed an inspection of Sentry Manufacturing, Inc. on Jul 21, 2026 in Miami Lakes, FL. 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). 18 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 21, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Miami Lakes, FL (United States)

Citations

IDCFRDescription
1564721 CFR 111.460(b)Hold - in-process material; temperature, humidity, light
1568121 CFR 111.315(d)Standard reference materials; criteria for selecting
1569821 CFR 111.320(a)Examination, testing; appropriate
1596321 CFR 111.113(b)(2)Quality control - reject; specification not met
1598621 CFR 111.123(b)(2)Quality control - batch, product specifications
2281021 CFR 111.353Written procedures - follow; manufacturing operations
2281821 CFR 111.10(b)Hygienic practices
2282321 CFR 111.15(b)Physical plant - clean and sanitary
2283621 CFR 111.27(a)Equipment - design - appropriate and suitable
2283721 CFR 111.27(d)Equipment - maintain - general
2284321 CFR 111.70(b)Specifications - components
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2285421 CFR 111.83(b)Reserve sample - container-closure system
2285921 CFR 111.103Written procedures - establish; quality control operations
2286921 CFR 111.140(b)(3)Records - material review, disposition, follow-up
2288821 CFR 111.210Master manufacturing record - record requirements
2289021 CFR 111.260Batch record - required information
2289721 CFR 111.325(b)Make and keep records - laboratory operations