Barr Laboratories LLC
FDA inspection history in Forest, Virginia, 2017 to 2022
- 3
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2018: one Form 483; 2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–18Two Form 483s, at Forest, Virginia.
- 2017The longest 483 on file: 4 observations over 5 pages at Forest, Virginia.
- 2022One Form 483, at Forest, Virginia.
Cited most
Across all Barr Laboratories observations on file
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.80General requirements1
The complete Barr Laboratories file.
All 3 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
Forest, Virginia
Three Form 483s · 2017 to 2022 · 6 observations
Latest: Form 483, Nov 4, 2022 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-04 | 483 Form 483 | Forest, Virginia | 1 | $99 |
| 2018-02-28 | 483 Form 483 | Forest, Virginia | 1 | $99 |
| 2017-04-14 | 483 Form 483 | Forest, Virginia | 4 | $99 |
Investigators on these documents
Eileen A. Liu (1)Fabian Chaparro (1)Jonathan W. Chapman (1)Marcus A. Ray (1)Simone E. Pitts (1)Thomas R. Withers (1)
FEI number 3000718267 · most recent document Nov 4, 2022
About Barr Laboratories LLC
How many FDA Form 483s has Barr Laboratories LLC received?
FDA Intel has 3 Form 483s on file for Barr Laboratories LLC; the most recent is dated Nov 4, 2022.
When was Barr Laboratories LLC last inspected by FDA?
The most recent FDA inspection document on file for Barr Laboratories LLC is a Form 483 dated Nov 4, 2022, for the site in Forest, Virginia.
What did FDA cite at Barr Laboratories LLC?
The regulations cited most in the observations on file for Barr Laboratories LLC are 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.