Ben Venue Laboratories, Inc.
FDA inspection history in Bedford, Ohio, 2011
- 2
- Form 483s
Every document, by year
- Form 483
2011: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2011Two Form 483s, at Bedford, Ohio.
- 2011The longest 483 on file: 10 observations over 12 pages at Bedford, Ohio.
Cited most
Across all Ben Venue Laboratories observations on file
- 21 CFR 211.113Control of microbiological contamination5
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.42Design and construction features1
The complete Ben Venue Laboratories file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Bedford, Ohio
Two Form 483s · 2011 · 14 observations
Latest: Form 483, Dec 2, 2011 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2011-12-02 | 483 Form 483 | Bedford, Ohio | 10 | $99 |
| 2011-05-25 | 483 Form 483 | Bedford, Ohio | 4 | $99 |
Investigators on these documents
Christopher T. Middendorf (1)Dell S. Moller (1)Dells Moller (1)Michael P. Sheehan (1)Paul A. Bennvagu (1)Sneha J. Padey (1)Thomas J. Arista (1)
FEI number 1519257 · most recent document Dec 2, 2011
About Ben Venue Laboratories, Inc.
How many FDA Form 483s has Ben Venue Laboratories, Inc. received?
FDA Intel has 2 Form 483s on file for Ben Venue Laboratories, Inc.; the most recent is dated Dec 2, 2011.
When was Ben Venue Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Ben Venue Laboratories, Inc. is a Form 483 dated Dec 2, 2011, for the site in Bedford, Ohio.
What did FDA cite at Ben Venue Laboratories, Inc.?
The regulations cited most in the observations on file for Ben Venue Laboratories, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 5 times; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.198 (Complaint files), 1 time.