FDA Inspection
H & P Industries, Inc.H & P Industries, Inc. – FDA Inspection, Oct 30, 2009
Record Details
This FDA Inspection record concerns H & P Industries, Inc., with an inspection on October 30, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- H & P Industries, Inc.
- Inspection Date
- October 30, 2009
- Product Type
- Drugs
View Company Profile
ID · 3cfd56e4-a267-4e90-a4da-1924d5cf10f7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 624826
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
- 21 CFR 211.25(c)Inadequate number of personnel
- 21 CFR 211.22(d)Procedures not in writing, fully followed
Full citation text and observation details available on the Dashboard.
Other FDA inspections of H & P Industries, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| March 28, 2011 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 7, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 4, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 10, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 18, 2010 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for H & P Industries, Inc.
- FDA Inspection 716726 - 2011-03-28
- FDA Inspection 700534 - 2011-01-07
- FDA Inspection 704694 - 2011-01-04
- FDA Inspection 697221 - 2010-11-10
- FDA Inspection 662690 - 2010-05-18
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.