FDA Inspection
R.A. McNeil CompanyR.A. McNeil Company – FDA Inspection, Apr 29, 2014
Record Details
This FDA Inspection record concerns R.A. McNeil Company, with an inspection on April 29, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- R.A. McNeil Company
- Inspection Date
- April 29, 2014
- Product Type
- Drugs
View Company Profile
ID · 766e1ebf-3358-4578-b228-a64f9c09dcb2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 875466
- FDA center
- Human Drugs
- Project area
- Unapproved and Misbranded Drugs
FDA Citations
6- 21 CFR 211.58Buildings not maintained in good state of repair
- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 211.46(b)Equipment for Environmental Control
- 21 CFR 211.142Written warehousing procedures established/followed
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.150Written distribution procedure
Full citation text and observation details available on the Dashboard.
Other FDA inspections of R.A. McNeil Company
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2026 | Not classified | New Orleans District Office |
Other documents for R.A. McNeil Company
- FDA Inspection 1307702 - 2026-02-03
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.