FDA Inspection
PulpoPulpo – FDA Inspection, Aug 7, 2025
Record Details
This FDA Inspection record concerns Pulpo, with an inspection on August 7, 2025, issued by the Denver District Office, covering foods & cosmetics.
View Company Profile
ID · 365a0612-15f8-4426-9d01-730830ecd6e5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1277784
- FDA center
- Foods & Cosmetics
- Project area
- Foodborne Biological Hazards
- Outcome
- Form 483 issued
FDA Citations
8- 21 CFR 111.260Batch record - required information
- 21 CFR 111.75(a)(2)(ii)(B)Component - certificate of analysis
- 21 CFR 111.70(b)Specifications - components
- 21 CFR 108.25(c)(1)Registration
- 21 CFR 114.83Scheduled process establishment
- 21 CFR 111.210Master manufacturing record - record requirements
- 21 CFR 111.75(h)Tests, examinations - scientifically valid
- 21 CFR 114.10Personnel
Full citation text and observation details available on the Dashboard.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.